Wednesday, 23 September 2026
Wednesday, 23 September 2026
- In brief
- 1Ebola vaccines teach the body the shape of the virus's outer protein, and the Ebola spreading in Congo has a different one
- 2Two treatments tested against Bundibugyo
- 3Congo's Ebola response misses its targets
- 4A vaccine made for Bundibugyo itself
- 5The outbreak spread for weeks unseen
- 6The first approved test for Bundibugyo
- 7US overdose deaths fell for a third year
- 8Nobody can name one reason deaths fell
- 9New street drugs naloxone often cannot reverse
- 10Cocaine and meth deaths without opioids rose
- 11A fentanyl shortage may explain part of the fall
- 12A second weight-loss pill approved
- 13Orforglipron beat oral semaglutide in diabetes
- 14The weight-loss pill tested in people over 65
- 15262 obesity drug trials compared
- 16A third company's weight-loss pill
- 17An unapproved drug given to one man
- 1843 studies, no Tylenol-autism link
- 191.5 million Danish children, no link
- 20A Taiwan result nobody can explain
- 21Tylenol use in emergency rooms dropped
- 22Plastic found in living brain tissue
- 23Doubts about plastic in the body
- 24Sports betting and binge drinking
- 25Betting on anything, from a phone
- 26Early strong treatment for Crohn's
- 27Approved, and harder to get
- 28A many-cancer blood test missed its goal
- 29The morning cancer trial was retracted
- 30Mpox reaches new countries
- 31Ethiopia's first Marburg outbreak ended
- 32The cruise ship hantavirus outbreak ended
- 33US addiction grants cut, then restored
- 34Britain's new clinical trial rules
- 35Few medical AI tools tested properly
- TruthThe truth, across the day
23 Sept · Mind & body · In brief
Mind & body · Wednesday, 23 September 2026
Mind & body, in brief
35 stories · 49 sources
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What is moving · 1 of 4
Drugs made for another target
Ervebo was made for the Zaire species of Ebola, not the Bundibugyo virus spreading in Congo.
What is moving · 2 of 4
Officials changing what people do
After US officials linked Tylenol to autism, emergency-room orders of it for pregnant women fell 16%.
What is moving · 3 of 4
Findings taken back or doubted
Nature Medicine retracted a trial in June that said cancer drugs given in the morning worked far better.
What is moving · 4 of 4
Who gets a new drug first
Families waiting for Rasonque, a pancreatic cancer drug, lost early access the day it was approved.
11 sources
Mind & body, in brief
- 6WHO emergency guidance on the use of licensed Ebola vaccine during Bundibugyo virus disease outbreaks
- 8WHO and Africa CDC welcome the allocation of Ebola vaccines to the Democratic Republic of the Congo
- 10Historic decline in U.S. overdose deaths threatened by changing street drug supply
- 11US drug overdose deaths involving stimulants without opioids continued to rise in 2024 - PMC
- 12Tylenol orders for pregnant people dropped after Trump linked the drug to autism
- 13New Policies Affecting Access to Mental Health Care
- 14Study on timing cancer treatments to the morning comes under fire
- 15'A bombshell': doubt cast on discovery of microplastics throughout human body
- 16The Fight Over Tylenol and Autism Just Got Messier
- 17FDA approved a revolutionary cancer drug. Insurance wasn't ready
- 18Eli Lilly gave mysterious access to weight loss drug to 79-year-old patient
Ebola vaccines teach the body the shape of the virus's outer protein, and the Ebola spreading in Congo has a different one
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Congo has confirmed 6,757 cases of Ebola caused by the Bundibugyo virus since the outbreak was declared on 15 May, and 3,267 of those people have died.
counted to 7 September in Congo, Uganda and one case in France; at least 1,611 people have recovered
Who is involved
The World Health Organization
the United Nations' health agency; it declared the outbreak a global health emergency on 17 May and said Ervebo should be used only inside research
Who is involved
Congo's Ministry of Public Health
Congo's health ministry; it declared the outbreak on 15 May and asked the global stockpile for vaccine doses
Why it matters
Watch the vaccine trial in Congo: the WHO says a clear benefit would let Ervebo's use widen quickly, and no benefit would send the money back to testing, isolation and Bundibugyo-specific vaccines.
What's really going on
Congo's Ebola outbreak is caused by a species of the virus with no vaccine and no approved treatment, and the one Ebola vaccine on the shelf was made for a different species.
What's really going on
Until a trial answers whether it works, the outbreak is being fought with testing, isolation and safe burials, and the CDC says most of those are below target.
Who pays
Health and frontline workers in Congo
They are first in line for a vaccine whose protection against Bundibugyo is unknown, and the WHO warns it could make people less careful.
Nobody knows yet
Whether Ervebo protects people against Bundibugyo at all.
No study in people has measured it. Animal studies suggest some protection against dying but little against infection, and a few vaccinated health workers who caught it and survived are too few to judge.
Nobody knows yet
How big the Ebola outbreak really is.
The WHO says part of the recent rise comes from more testing and catching up on unreported data. The CDC found only 72% of suspected cases tested and most new cases outside known contact chains.
Nobody knows yet
When the outbreak began.
The first known case fell ill on 24 April, but a CDC model puts the jump from animals to people in mid to late February, and early cases were logged as malaria or typhoid.
The short version
That's the story in short.
The whole story has 13 more parts.
or swipe up for the next storyor scroll on for the next story ↓
The whole story, in 13 parts ↓
Part 1 of 13 · Who else is involved
Merck
the drug company that makes Ervebo, the only licensed Ebola vaccine, which was made for the Zaire species
Part 1 of 13 · Who else is involved
The University of Oxford
the UK university whose scientists made a vaccine aimed at Bundibugyo itself; it is being tested for safety in 50 healthy volunteers
Part 2 of 13 · How it unfolded
Feb 2026
a CDC computer model puts the virus's jump from animals to people in mid to late February
17 May
the WHO declares a global health emergency
Part 2 of 13 · How it unfolded
17 May
the WHO declares a global health emergency
2 Jul
a trial of two treatments enrols its first patient
Part 3 of 13
It is the second largest Ebola outbreak ever recorded, behind West Africa in 2014-2016, when more than 11,000 people died.
Part 4 of 13
Confirmed cases in Congo rose from 210 on 31 May to 1,406 on 2 July, 5,458 on 21 August and 6,757 on 7 September.
Part 5 of 13
The only licensed Ebola vaccine, Ervebo, made by the drug company Merck, trains the body to recognise the glycoprotein, the protein on the outside of the virus.
Part 6 of 13
Ervebo was made for a different species, the Zaire Ebola virus.
Part 6 of 13
The two viruses' outer proteins share only about 60 to 65% of their building blocks.
Part 7 of 13
People given Ervebo make about five times less antibody that sticks to Bundibugyo's outer protein than to Zaire's.
Part 8 of 13
In ferrets given the vaccine, the average antibody reading was 16,582 against Bundibugyo's protein and 56,554 against Zaire's.
Part 9 of 13
Studies in monkeys and ferrets suggest the vaccine gives some protection against dying of Bundibugyo, but little or none against the virus multiplying in the blood or against falling ill.
Part 10 of 13
On 31 August the World Health Organization said Ervebo should be used against Bundibugyo only inside research, because no study has yet measured whether it protects people.
Part 11 of 13
Congo asked the global vaccine stockpile for doses, and 70,000 were released: 20,000 for a trial and 50,000 for health and frontline workers.
Part 12 of 13
The first known case was a health worker in Bunia who fell ill on 24 April.
Part 12 of 13
Early cases were mistaken for typhoid and malaria.
Part 13 of 13
About one million people forced from their homes live in Ituri province alone, and armed conflict there slows the finding of cases and the tracing of their contacts.
10 sources
Ebola vaccines teach the body the shape of the virus's outer protein, and the Ebola spreading in Congo has a different one
- 1Ebola disease caused by Bundibugyo virus - Democratic Republic of the Congo (Disease Outbreak News, 7 September 2026)
- 2Notes from the Field: Characteristics and Monitoring of the 2026 Outbreak of Ebola Disease Caused by Bundibugyo Virus - Democratic Republic of the Congo, August 2026
- 3Ebola in DR Congo: Vaccine trial to start as WHO warns about speed of infections
- 4Four health workers recover from Ebola in the Democratic Republic of the Congo
- 5WHO adds first diagnostic test for Ebola Bundibugyo virus to its Emergency Use Listing
- 6WHO emergency guidance on the use of licensed Ebola vaccine during Bundibugyo virus disease outbreaks
- 7Antibodies Cross-Reactive with Bundibugyo Virus in Ferrets Vaccinated with Ebola Virus Vaccine - Volume 32, Number 8-August 2026 - Emerging Infectious Diseases journal
- 8WHO and Africa CDC welcome the allocation of Ebola vaccines to the Democratic Republic of the Congo
- 9Ebola disease caused by Bundibugyo virus, Democratic Republic of the Congo and Uganda (Disease Outbreak News, 15 May 2026)
- 19Modeled Scenario Projections for the Ebola Disease Outbreak Caused by Bundibugyo Virus, 2026
The full story
Ebola vaccines teach the body the shape of the virus's outer protein, and the Ebola spreading in Congo has a different one
Congo has confirmed 6,757 cases of Ebola caused by the Bundibugyo virus since the outbreak was declared on 15 May, and 3,267 of those people have died.
It is the second largest Ebola outbreak ever recorded, behind West Africa in 2014-2016, when more than 11,000 people died.
Confirmed cases in Congo rose from 210 on 31 May to 1,406 on 2 July, 5,458 on 21 August and 6,757 on 7 September.
The only licensed Ebola vaccine, Ervebo, made by the drug company Merck, trains the body to recognise the glycoprotein, the protein on the outside of the virus.
Ervebo was made for a different species, the Zaire Ebola virus. The two viruses' outer proteins share only about 60 to 65% of their building blocks.
People given Ervebo make about five times less antibody that sticks to Bundibugyo's outer protein than to Zaire's.
In ferrets given the vaccine, the average antibody reading was 16,582 against Bundibugyo's protein and 56,554 against Zaire's.
Studies in monkeys and ferrets suggest the vaccine gives some protection against dying of Bundibugyo, but little or none against the virus multiplying in the blood or against falling ill.
On 31 August the World Health Organization said Ervebo should be used against Bundibugyo only inside research, because no study has yet measured whether it protects people.
Congo asked the global vaccine stockpile for doses, and 70,000 were released: 20,000 for a trial and 50,000 for health and frontline workers.
The first known case was a health worker in Bunia who fell ill on 24 April. Early cases were mistaken for typhoid and malaria.
About one million people forced from their homes live in Ituri province alone, and armed conflict there slows the finding of cases and the tracing of their contacts.
Why it matters. Watch the vaccine trial in Congo: the WHO says a clear benefit would let Ervebo's use widen quickly, and no benefit would send the money back to testing, isolation and Bundibugyo-specific vaccines.
Two treatments tested against Bundibugyo
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A trial called PARTNERS began enrolling Ebola patients in Congo on 2 July.
It tests two drugs against the Bundibugyo virus, alone and together: MBP134, a lab-made antibody, and remdesivir, an antiviral drug.
Treatments exist for Zaire Ebola, but none is approved for Bundibugyo.
Patients who join are followed for at least 28 days.
Why it matters
Until a drug is proven, the WHO says people who reach a treatment centre early have a better chance of surviving.
Why it matters
Four nurses in Bunia recovered that way in late May.
How it works
A treatment fits the exact shape it was made for
How it works
Vaccines, antidotes and pills all work by fitting one precise shape, so a virus or a street drug with a different shape can get past them.
How it works · step 1 of 5
A vaccine or drug is built to grip one particular molecule
How it works · step 2 of 5
It works when it meets that molecule
How it works · step 3 of 5
A related virus or street drug is built slightly differently
How it works · step 4 of 5
The grip is weaker, or there is none
How it works · step 5 of 5
Only a new trial shows how much protection is left
The twist
The Ebola vaccine did not get weaker. The virus it meets in Congo has a different outer protein from the one the vaccine copies.
The picture
Average antibody readings in ferrets given the Ebola vaccine. The reading against Bundibugyo is less than a third of the reading against the virus the vaccine was made for.
Seen the same day
Naloxone is made to reverse opioid overdoses. Medetomidine is a sedative, not an opioid, so the new street mixes often do not respond to it.
Seen the same day
The tools behind the fall in overdose deaths were mostly aimed at opioids. Deaths from stimulants taken without any opioid rose slightly while fentanyl deaths fell.
Seen the same day
Treatments exist for Zaire Ebola, but none has been shown to work across every type of Ebola, so Bundibugyo patients need drugs tested against their own virus.
Seen the same day
Here the fit was kept and the rest was changed.
Seen the same day
Orforglipron aims at the same GLP-1 target as Wegovy but is built as a small molecule, so it needs no 30-minute wait before food.
The catch
A near fit can still help.
The catch
In monkeys and ferrets Ervebo gave some protection against dying of Bundibugyo, and only the trial in Congo can say how much of that carries over to people.
The whole
The global stockpile was filled with a vaccine made for Zaire Ebola.
The whole
The nurses and families in Ituri got a different species, and they are the people waiting for the trial to answer.
The whole
Anyone who takes a medicine is relying on the same kind of match between a drug and the target it was made for.
Good news
At least 1,611 people have recovered from Bundibugyo Ebola, a disease with no approved treatment.
The full story
Two treatments tested against Bundibugyo
A trial called PARTNERS began enrolling Ebola patients in Congo on 2 July.
Why it matters. Until a drug is proven, the WHO says people who reach a treatment centre early have a better chance of surviving. Four nurses in Bunia recovered that way in late May.
Congo's Ebola response misses its targets
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A report from the US Centers for Disease Control and Prevention (CDC), published on 10 September, measured Congo's Ebola response against five targets up to 21 August.
Only 15 to 20% of new cases had been known contacts of earlier cases, against a target above 90%.
Fewer than half of the affected health zones had a team for safe burials.
Why it matters
When most new cases come from people nobody was watching, the virus is spreading along chains the response cannot see.
Why it matters
Bodies of people who die at home can pass Ebola on at funerals, which is why burial teams are one of the five targets.
Who pays
Families in Ituri and North Kivu
59% of Ebola deaths happened outside a treatment unit, and fewer than half of affected health zones had a safe burial team.
1 source
Congo's Ebola response misses its targets
The full story
Congo's Ebola response misses its targets
A report from the US Centers for Disease Control and Prevention (CDC), published on 10 September, measured Congo's Ebola response against five targets up to 21 August.
Why it matters. When most new cases come from people nobody was watching, the virus is spreading along chains the response cannot see. Bodies of people who die at home can pass Ebola on at funerals, which is why burial teams are one of the five targets.
A vaccine made for Bundibugyo itself
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Oxford scientists built a vaccine aimed at Bundibugyo, called ChAdOx1 Ebola BDBV, with the same method as the Oxford-AstraZeneca Covid vaccine.
Its first trial in people began in Oxford in July, and University Hospital Southampton joined on 2 September.
It will give 50 healthy adults aged 18 to 55 one or two doses or a dummy injection, and track safety and immune response for a year.
In June, CEPI gave about $62m to three Bundibugyo vaccine projects.
Why it matters
This first trial checks safety, not whether the vaccine stops Ebola. The WHO says vaccines made for Bundibugyo may work better than Ervebo, which was made for another species.
Who gains
Bundibugyo vaccine developers
CEPI gave about $62m to three projects, and the WHO says vaccines made for Bundibugyo may outperform Ervebo.
3 sources
A vaccine made for Bundibugyo itself
The full story
A vaccine made for Bundibugyo itself
Oxford scientists built a vaccine aimed at Bundibugyo, called ChAdOx1 Ebola BDBV, with the same method as the Oxford-AstraZeneca Covid vaccine.
Why it matters. This first trial checks safety, not whether the vaccine stops Ebola. The WHO says vaccines made for Bundibugyo may work better than Ervebo, which was made for another species.
The outbreak spread for weeks unseen
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Congo declared the outbreak on 15 May, when 246 suspected cases and 80 deaths had already been counted.
The first alert, which reached the WHO on 5 May, described an unknown illness in Mongbwalu, in Ituri, that had killed four health workers within four days.
A CDC computer model published in June suggested the virus jumped from an animal to a person in mid to late February.
An infectious disease doctor at Emory University said the size of the first count suggested it had been going on for weeks.
Why it matters
Every week an outbreak goes unrecognised is a week with no isolation or contact tracing.
Why it matters
Bundibugyo's first symptoms, such as fever and tiredness, are hard to tell from malaria without a laboratory test.
4 sources
The outbreak spread for weeks unseen
- 1Ebola disease caused by Bundibugyo virus - Democratic Republic of the Congo (Disease Outbreak News, 7 September 2026)
- 9Ebola disease caused by Bundibugyo virus, Democratic Republic of the Congo and Uganda (Disease Outbreak News, 15 May 2026)
- 19Modeled Scenario Projections for the Ebola Disease Outbreak Caused by Bundibugyo Virus, 2026
- 24This Ebola outbreak raises questions about when it all began - and the U.S. response
The full story
The outbreak spread for weeks unseen
Congo declared the outbreak on 15 May, when 246 suspected cases and 80 deaths had already been counted.
Why it matters. Every week an outbreak goes unrecognised is a week with no isolation or contact tracing. Bundibugyo's first symptoms, such as fever and tiredness, are hard to tell from malaria without a laboratory test.
The first approved test for Bundibugyo
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On 2 July the WHO added the first test for the Bundibugyo virus to its emergency list, which lets UN agencies and governments buy it knowing it meets quality standards.
The test finds the virus's genetic material in a blood sample.
Congo's testing had relied on a few laboratories, mainly in Kinshasa and Goma.
Why it matters
Without a test, Ebola is easily mistaken for malaria or typhoid, and cases are missed.
Why it matters
By late August the CDC found only 72% of checked alerts about possible cases had been tested.
2 sources
The first approved test for Bundibugyo
The full story
The first approved test for Bundibugyo
On 2 July the WHO added the first test for the Bundibugyo virus to its emergency list, which lets UN agencies and governments buy it knowing it meets quality standards.
Why it matters. Without a test, Ebola is easily mistaken for malaria or typhoid, and cases are missed. By late August the CDC found only 72% of checked alerts about possible cases had been tested.
US overdose deaths fell for a third year
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About 70,000 people in the United States died of drug overdoses in 2025, around 14% fewer than in 2024, according to early government figures released in May.
It was the third yearly fall in a row, the longest decline in decades.
Seven states went up, including Arizona, Colorado and New Mexico, each by 10% or more.
Why it matters
Roughly 11,300 fewer people died than the year before.
Who pays
People using drugs in Arizona, Colorado and New Mexico
Overdose deaths rose 10% or more there in 2025 while most states fell.
Good news
About 70,000 people died of drug overdoses in the United States in 2025, roughly 11,300 fewer than the year before and the third yearly fall in a row.
The full story
US overdose deaths fell for a third year
About 70,000 people in the United States died of drug overdoses in 2025, around 14% fewer than in 2024, according to early government figures released in May.
Why it matters. Roughly 11,300 fewer people died than the year before.
Nobody can name one reason deaths fell
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A Commonwealth Fund report on 3 September asked addiction officials in at least two dozen US states and other countries why overdose deaths fell.
Every one of them said no single thing did it.
They named naloxone, a spray that reverses opioid overdoses, wider use of addiction medicines such as methadone, and treatment in prisons.
Virginia saw deaths fall 40% from 2023 to 2024 after a plan to put naloxone everywhere.
Why it matters
Deaths also fell in Scotland and Canada in 2024, but Scotland's may have risen again in 2025.
Why it matters
Experts named cuts to Medicaid, the US health insurance for people on low incomes, as the biggest threat.
Nobody knows yet
Why US overdose deaths fell.
Officials credit naloxone, addiction medicines and prison treatment, while other researchers point to weaker fentanyl after China's rule changes. Nobody has measured how much each did.
Nobody knows yet
Whether the overdose fall will last.
New sedatives resist naloxone, Scotland's deaths may have risen again in 2025, and Medicaid cuts are due.
The full story
Nobody can name one reason deaths fell
A Commonwealth Fund report on 3 September asked addiction officials in at least two dozen US states and other countries why overdose deaths fell.
Why it matters. Deaths also fell in Scotland and Canada in 2024, but Scotland's may have risen again in 2025. Experts named cuts to Medicaid, the US health insurance for people on low incomes, as the biggest threat.
New street drugs naloxone often cannot reverse
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US street drugs now hold a fast-changing mix of industrial chemicals that chemists call a synthetic soup, NPR reported in April.
They include medetomidine, a powerful sedative that can damage the heart, and new opioids such as cychlorphine and nitazenes, often stronger than fentanyl.
These mixes often do not respond to naloxone, the standard drug for reversing an opioid overdose.
Why it matters
A US government chemist said a substance never seen before turns up every month or two.
Why it matters
Nobody buying street drugs can know what a batch holds, and naloxone is made to reverse opioids.
How it works
Naloxone is made to reverse opioid overdoses. Medetomidine is a sedative, not an opioid, so the new street mixes often do not respond to it.
The idea, in story 2: A treatment fits the exact shape it was made for →1 source
New street drugs naloxone often cannot reverse
The full story
New street drugs naloxone often cannot reverse
US street drugs now hold a fast-changing mix of industrial chemicals that chemists call a synthetic soup, NPR reported in April.
Why it matters. A US government chemist said a substance never seen before turns up every month or two.
Cocaine and meth deaths without opioids rose
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US overdose death rates fell 27.9% from their 2022 peak to 2024, mostly because fewer people died from fentanyl.
But deaths from cocaine or methamphetamine taken without any opioid rose slightly from 2023 to 2024, by 1.7% and 2.4%.
Methamphetamine deaths rose among Black, Native American and over-55 groups.
Why it matters
The tools behind the overall fall were mostly aimed at opioids. The authors say prevention now has to reach the harms of stimulants too.
How it works
The tools behind the fall in overdose deaths were mostly aimed at opioids. Deaths from stimulants taken without any opioid rose slightly while fentanyl deaths fell.
The idea, in story 2: A treatment fits the exact shape it was made for →1 source
Cocaine and meth deaths without opioids rose
The full story
Cocaine and meth deaths without opioids rose
US overdose death rates fell 27.9% from their 2022 peak to 2024, mostly because fewer people died from fentanyl.
Why it matters. The tools behind the overall fall were mostly aimed at opioids. The authors say prevention now has to reach the harms of stimulants too.
A fentanyl shortage may explain part of the fall
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Overdose deaths fell 27% in 2024 to around 80,000, the largest one-year drop ever recorded.
A paper in the journal Science by University of Maryland researchers pointed to the drug supply.
It argued that rule changes in China cut the chemicals used to make fentanyl, so the drug got harder to make and weaker.
US drug agents had reported fentanyl strength rising early in the pandemic and falling after 2022.
Why it matters
If weaker fentanyl did much of the work, deaths could climb again when the supply changes.
Why it matters
Researchers named a shift in the drug supply as one thing that could reverse the fall.
2 sources
A fentanyl shortage may explain part of the fall
The full story
A fentanyl shortage may explain part of the fall
Overdose deaths fell 27% in 2024 to around 80,000, the largest one-year drop ever recorded.
Why it matters. If weaker fentanyl did much of the work, deaths could climb again when the supply changes. Researchers named a shift in the drug supply as one thing that could reverse the fall.
A second weight-loss pill approved
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The US Food and Drug Administration (FDA) approved Eli Lilly's daily weight-loss pill orforglipron, sold as Foundayo, on 1 April.
It acts on the same target as the weekly injections Wegovy and Zepbound, the body's receptor for a hormone called GLP-1.
In a 72-week trial in people with type 2 diabetes, the highest dose took off almost 10% of body weight.
Why it matters
Pills are easier to ship than injections and need no cold storage.
Why it matters
In separate trials the top dose of the Wegovy pill took off about 17% and the tirzepatide injection about 21%.
Why it matters
Who gains
Eli Lilly
Foundayo was approved under a new FDA voucher scheme that gives speedy reviews, the fastest approval of a new medicine in decades.
3 sources
A second weight-loss pill approved
The full story
A second weight-loss pill approved
The US Food and Drug Administration (FDA) approved Eli Lilly's daily weight-loss pill orforglipron, sold as Foundayo, on 1 April.
Why it matters. Pills are easier to ship than injections and need no cold storage.
Orforglipron beat oral semaglutide in diabetes
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A trial of 1,698 people with type 2 diabetes compared Lilly's orforglipron with Novo's oral semaglutide, the pill Rybelsus, for 52 weeks.
A standard blood sugar marker fell by nearly 2 points on the top orforglipron dose, against nearly 1.5 on semaglutide.
People also lost more weight on orforglipron, but fewer of them stayed on it.
Why it matters
It is a direct comparison of two pills rather than two separate trials.
Why it matters
Doctors hope pills like these could let some people with diabetes rely less on insulin, which can cause weight gain.
1 source
Orforglipron beat oral semaglutide in diabetes
The full story
Orforglipron beat oral semaglutide in diabetes
A trial of 1,698 people with type 2 diabetes compared Lilly's orforglipron with Novo's oral semaglutide, the pill Rybelsus, for 52 weeks.
Why it matters. It is a direct comparison of two pills rather than two separate trials. Doctors hope pills like these could let some people with diabetes rely less on insulin, which can cause weight gain.
The weight-loss pill tested in people over 65
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A new analysis looked at 616 people aged 65 or over in two orforglipron trials, published in September in the journal Obesity Pillars.
After 72 weeks those on the top dose lost 12 to 13% of their body weight, against about 2% on a dummy pill.
Orforglipron is a small molecule, not a peptide, the protein-like chain the Wegovy pill is made of.
Why it matters
The Wegovy pill has to be taken 30 minutes before any food, and orforglipron has no such rule.
How it works
Here the fit was kept and the rest was changed. Orforglipron aims at the same GLP-1 target as Wegovy but is built as a small molecule, so it needs no 30-minute wait before food.
The idea, in story 2: A treatment fits the exact shape it was made for →2 sources
The weight-loss pill tested in people over 65
The full story
The weight-loss pill tested in people over 65
A new analysis looked at 616 people aged 65 or over in two orforglipron trials, published in September in the journal Obesity Pillars.
Why it matters. The Wegovy pill has to be taken 30 minutes before any food, and orforglipron has no such rule.
262 obesity drug trials compared
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A review in The BMJ this year pooled 262 trials with 99,791 people, testing 19 weight-loss drugs.
After a year, tirzepatide took off about 14.9% of body weight compared with diet and exercise alone, and orforglipron about 9.9%.
Injected semaglutide was the only drug linked to fewer deaths from any cause.
Why it matters
Tirzepatide cut the most fat, 25.7%, but also the most muscle and other lean tissue, 8.3%.
Why it matters
No drug clearly improved quality of life by more than the smallest change patients notice.
1 source
262 obesity drug trials compared
The full story
262 obesity drug trials compared
A review in The BMJ this year pooled 262 trials with 99,791 people, testing 19 weight-loss drugs.
Why it matters. Tirzepatide cut the most fat, 25.7%, but also the most muscle and other lean tissue, 8.3%.
A third company's weight-loss pill
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Structure Therapeutics, a US biotech company, reported results for its daily weight-loss pill on 16 March.
After 44 weeks, people lost about 16% of their body weight compared with a dummy pill.
The company is racing Eli Lilly and Novo Nordisk to sell a pill version of the GLP-1 injections.
Why it matters
Lilly's orforglipron produced about 11% in its own 72-week trial, reported last year.
1 source
A third company's weight-loss pill
The full story
A third company's weight-loss pill
Structure Therapeutics, a US biotech company, reported results for its daily weight-loss pill on 16 March.
Why it matters. Lilly's orforglipron produced about 11% in its own 72-week trial, reported last year.
An unapproved drug given to one man
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Eli Lilly and the FDA let one 79-year-old man receive retatrutide, an experimental weight-loss drug, STAT reported on 23 June.
He got it through compassionate use, a route meant for patients with serious and immediately life-threatening illness.
Three sources said the request, made in April, drew interest from top health officials, suggesting the man was well connected.
Why it matters
Retatrutide has produced weight loss on the scale of stomach surgery in trials, and millions of Americans are waiting for it.
1 source
An unapproved drug given to one man
The full story
An unapproved drug given to one man
Eli Lilly and the FDA let one 79-year-old man receive retatrutide, an experimental weight-loss drug, STAT reported on 23 June.
Why it matters. Retatrutide has produced weight loss on the scale of stomach surgery in trials, and millions of Americans are waiting for it.
43 studies, no Tylenol-autism link
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A review in the Lancet in January found that paracetamol in pregnancy, sold as Tylenol in the US, did not raise the risk of autism, ADHD or intellectual disability.
Researchers across Europe narrowed thousands of papers to the 43 studies least likely to be biased.
Studies comparing brothers and sisters, one exposed in the womb and one not, found the exposed child was no more likely to have autism.
In September 2025 US officials had advised using it only if needed.
Why it matters
Doctors use paracetamol in pregnancy because fever raises the risk of birth defects, and ibuprofen and opioids carry their own risks to the baby.
Why it matters
The US health department said the study did not refute other research.
1 source
43 studies, no Tylenol-autism link
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43 studies, no Tylenol-autism link
A review in the Lancet in January found that paracetamol in pregnancy, sold as Tylenol in the US, did not raise the risk of autism, ADHD or intellectual disability.
Why it matters. Doctors use paracetamol in pregnancy because fever raises the risk of birth defects, and ibuprofen and opioids carry their own risks to the baby.
1.5 million Danish children, no link
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A Danish study published on 13 April tracked more than 1.5 million children born between 1997 and 2022, including 31,098 exposed to paracetamol in the womb.
Autism was diagnosed in 1.8% of the exposed children and 3% of the others.
- 1Exposed to paracetamol in the womb1.8%
- 2Not exposed3%
Why it matters
Comparing siblings matters because brothers and sisters share much of their genes and home life. The Swedish result suggests autism is strongly genetic, which other studies had already shown.
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1.5 million Danish children, no link
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1.5 million Danish children, no link
A Danish study published on 13 April tracked more than 1.5 million children born between 1997 and 2022, including 31,098 exposed to paracetamol in the womb.
- 1Exposed to paracetamol in the womb1.8%
- 2Not exposed3%
Why it matters. Comparing siblings matters because brothers and sisters share much of their genes and home life. The Swedish result suggests autism is strongly genetic, which other studies had already shown.
A Taiwan result nobody can explain
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A Taiwanese study of more than 2 million children born from 2004 to 2015, published in JAMA Pediatrics in March, found a link between paracetamol in pregnancy and autism or ADHD.
The link disappeared when siblings were compared, as in Sweden and Japan.
When only the younger one had, its risk fell.
Why it matters
The authors used the oddity to question sibling studies in general, including their own. A Swedish researcher called it a local quirk that does not overturn the other results.
Nobody knows yet
Why the Taiwan sibling results pointed in opposite directions.
Older exposed siblings showed more risk and younger exposed siblings less, and the authors offered no explanation. Large studies from Sweden, Japan and Denmark found no link.
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A Taiwan result nobody can explain
The full story
A Taiwan result nobody can explain
A Taiwanese study of more than 2 million children born from 2004 to 2015, published in JAMA Pediatrics in March, found a link between paracetamol in pregnancy and autism or ADHD.
Why it matters. The authors used the oddity to question sibling studies in general, including their own. A Swedish researcher called it a local quirk that does not overturn the other results.
Tylenol use in emergency rooms dropped
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After US officials linked Tylenol to autism in September 2025, emergency-room orders of it for pregnant women fell 16%, then settled 10% lower over 12 weeks.
There was no significant drop for women who were not pregnant.
The study was published in the Lancet on 5 March.
Why it matters
Paracetamol treats fever in pregnancy, and an untreated fever carries its own risks to the pregnant woman and to the baby's developing brain.
Who gains
Makers and prescribers of leucovorin
Prescriptions of the old cancer drug for children rose 71% in the weeks after US officials promoted it for autism.
Who pays
Pregnant women with a fever in the US
Emergency-room paracetamol orders for them fell 16% after the autism warning, and an untreated fever carries its own risks.
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Tylenol use in emergency rooms dropped
The full story
Tylenol use in emergency rooms dropped
After US officials linked Tylenol to autism in September 2025, emergency-room orders of it for pregnant women fell 16%, then settled 10% lower over 12 weeks.
Why it matters. Paracetamol treats fever in pregnancy, and an untreated fever carries its own risks to the pregnant woman and to the baby's developing brain.
Plastic found in living brain tissue
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Researchers analysed 156 samples from 113 people having brain tumours removed, and 35 samples from five healthy people who had died.
Tiny plastic particles turned up in 99.4% of the tumour patients' samples and in every healthy one.
Tissue around the tumours held more than healthy brain, perhaps because tumours damage the barrier that protects the brain.
Why it matters
More plastic went with faster-growing tumours. The authors say this shows the particles are present, and that more research is needed to learn whether they cause disease.
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Plastic found in living brain tissue
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Plastic found in living brain tissue
Researchers analysed 156 samples from 113 people having brain tumours removed, and 35 samples from five healthy people who had died.
Why it matters. More plastic went with faster-growing tumours. The authors say this shows the particles are present, and that more research is needed to learn whether they cause disease.
Doubts about plastic in the body
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Scientists told the Guardian in January that many reports of tiny plastics in the brain, arteries, testes and blood may come from contamination or false readings.
The Guardian counted seven studies challenged in their own journals.
The brain is about 60% fat.
Why it matters
Nobody doubts that plastic pollutes food, water and air. What is in doubt is how much is inside people, and researchers warned that wrong numbers could lead to wrong rules.
Nobody knows yet
How much plastic is really in the human brain.
The brain tumour study used a method that heats tissue into gas, and critics say fat in tissue can give the same signal as some plastics.
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Doubts about plastic in the body
The full story
Doubts about plastic in the body
Scientists told the Guardian in January that many reports of tiny plastics in the brain, arteries, testes and blood may come from contamination or false readings.
Why it matters. Nobody doubts that plastic pollutes food, water and air. What is in doubt is how much is inside people, and researchers warned that wrong numbers could lead to wrong rules.
Sports betting and binge drinking
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A study reported in March found that US men aged 35 or under who already binge drank did so 10% more often after online sports betting became legal in their state.
Binge drinking meant five or more drinks in one sitting.
The figures come from the men's own reports of their drinking.
Why it matters
The senior author, an economist, says the study shows a cause but does not test the reason behind it.
Why it matters
A 2024 survey found one in four US men aged 30 or under bets on sports online.
1 source
Sports betting and binge drinking
The full story
Sports betting and binge drinking
A study reported in March found that US men aged 35 or under who already binge drank did so 10% more often after online sports betting became legal in their state.
Why it matters. The senior author, an economist, says the study shows a cause but does not test the reason behind it.
Betting on anything, from a phone
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Prediction markets such as Kalshi and Polymarket let people bet on almost any event, and they are regulated as financial markets, not as gambling.
Anyone aged 18 or over can join.
During this year's Super Bowl, Kalshi handled more than $1bn in trades.
Why it matters
Gambling disorder is the only behavioural addiction in the main US psychiatric manual, and it shares brain features with drug addiction.
Why it matters
Fewer than one in ten people with gambling problems seeks treatment.
Who gains
Kalshi and Polymarket
They are regulated as financial markets rather than as gambling, which lets anyone aged 18 or over bet on almost any event.
Who pays
People recovering from gambling problems
In Pennsylvania, requests to be blocked from gambling apps rose from 2,200 in 2023 to 3,500 in 2024.
Nobody knows yet
Whether prediction markets cause gambling problems.
The markets are new, and a Harvard researcher says there is little research on their users so far.
The full story
Betting on anything, from a phone
Prediction markets such as Kalshi and Polymarket let people bet on almost any event, and they are regulated as financial markets, not as gambling.
Why it matters. Gambling disorder is the only behavioural addiction in the main US psychiatric manual, and it shares brain features with drug addiction.
Early strong treatment for Crohn's
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A UK trial followed more than 350 people with Crohn's disease, a lifelong inflammation of the gut, for about five years after diagnosis.
Some started strong drugs such as infliximab straight away, instead of waiting until the disease got worse.
They were half as likely to be admitted to hospital, and five times less likely to need abdominal surgery.
Why it matters
Current guidance usually saves these drugs for people whose disease is already more severe. About one person in 350 in the UK has Crohn's.
Who gains
People newly diagnosed with Crohn's disease in the UK
The PROFILE trial gives doctors evidence to start strong drugs at diagnosis, which halved hospital admissions over five years.
Good news
In a UK trial of more than 350 people newly diagnosed with Crohn's disease, those given strong treatment straight away were five times less likely to need abdominal surgery over five years.
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Early strong treatment for Crohn's
The full story
Early strong treatment for Crohn's
A UK trial followed more than 350 people with Crohn's disease, a lifelong inflammation of the gut, for about five years after diagnosis.
Why it matters. Current guidance usually saves these drugs for people whose disease is already more severe. About one person in 350 in the UK has Crohn's.
Approved, and harder to get
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The FDA approved Rasonque, a pancreatic cancer drug made by Revolution Medicines, in August.
Approval shut the company's early-access programme at once, but insurers take weeks or months to start paying for a new drug.
Families already in line, such as that of nurse Kelsey Solano, whose husband has advanced pancreatic cancer, were left waiting.
Why it matters
Rasonque has been shown to nearly double how long patients live on average, and pancreatic cancer is one of the most aggressive cancers.
Who pays
Pancreatic cancer patients waiting for Rasonque
Approval closed the early-access programme before insurers were ready to pay, and one Medicare patient was refused.
1 source
Approved, and harder to get
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Approved, and harder to get
The FDA approved Rasonque, a pancreatic cancer drug made by Revolution Medicines, in August.
Why it matters. Rasonque has been shown to nearly double how long patients live on average, and pancreatic cancer is one of the most aggressive cancers.
A many-cancer blood test missed its goal
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The NHS-Galleri trial gave 143,000 people in England aged 50 to 77 either usual care or a yearly blood test for many cancers at once.
After three rounds it did not cut the combined number of stage 3 and 4 cancers, its main goal.
Of people who tested positive, 52% really had cancer.
Why it matters
Stage 3 cancer is often still treatable with surgery or radiation, so an oncologist writing in STAT argued the shift from stage 4 matters.
Nobody knows yet
Whether the Galleri blood test saves lives.
The NHS trial found fewer stage 4 cancers but more stage 3 ones, and its combined goal was missed, so deaths prevented is still unmeasured.
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A many-cancer blood test missed its goal
The full story
A many-cancer blood test missed its goal
The NHS-Galleri trial gave 143,000 people in England aged 50 to 77 either usual care or a yearly blood test for many cancers at once.
Why it matters. Stage 3 cancer is often still treatable with surgery or radiation, so an oncologist writing in STAT argued the shift from stage 4 matters.
The morning cancer trial was retracted
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In February a trial in Nature Medicine reported that lung cancer patients given immunotherapy in the morning did far better than those treated in the afternoon.
Other scientists soon pointed to inconsistencies in its data.
Why it matters
The result had raised the hope that simply moving infusions to the morning could make cancer drugs work better.
1 source
The morning cancer trial was retracted
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The morning cancer trial was retracted
In February a trial in Nature Medicine reported that lung cancer patients given immunotherapy in the morning did far better than those treated in the afternoon.
Why it matters. The result had raised the hope that simply moving infusions to the morning could make cancer drugs work better.
Mpox reaches new countries
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The WHO's mpox report of 23 January counted 52,845 confirmed cases and 215 deaths in 98 countries during 2025.
Clade Ib, one form of the virus, was reported for the first time in Czechia, Israel, Madagascar, Nepal and France's island of Mayotte.
Madagascar had an outbreak spreading inside the country from December.
Why it matters
The global emergency over mpox ended in September 2025, but the virus keeps reaching new countries.
The full story
Mpox reaches new countries
The WHO's mpox report of 23 January counted 52,845 confirmed cases and 215 deaths in 98 countries during 2025.
Why it matters. The global emergency over mpox ended in September 2025, but the virus keeps reaching new countries.
Ethiopia's first Marburg outbreak ended
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Ethiopia declared its first ever outbreak of Marburg virus, which causes an illness like Ebola, on 14 November 2025 in the southern town of Jinka.
There were 14 confirmed cases, nine of whom died, plus five probable cases, all of whom died.
It was declared over on 26 January, after 42 days with no new case.
Why it matters
There is no approved vaccine or treatment for Marburg either. It was stopped by following contacts, testing and safe burials.
Good news
Ethiopia's first ever Marburg outbreak was declared over on 26 January, after 42 days with no new case.
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Ethiopia's first Marburg outbreak ended
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Ethiopia's first Marburg outbreak ended
Ethiopia declared its first ever outbreak of Marburg virus, which causes an illness like Ebola, on 14 November 2025 in the southern town of Jinka.
Why it matters. There is no approved vaccine or treatment for Marburg either. It was stopped by following contacts, testing and safe burials.
The cruise ship hantavirus outbreak ended
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The WHO declared the hantavirus outbreak linked to the cruise ship MV Hondius over on 2 July.
Health authorities followed more than 650 contacts in 33 countries and territories.
Why it matters
The WHO is now running a study in 21 countries on how the disease develops, to help build tests, drugs and vaccines for future outbreaks.
Good news
The WHO declared the hantavirus outbreak on the cruise ship MV Hondius over on 2 July, after health authorities followed more than 650 contacts in 33 countries and territories.
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The cruise ship hantavirus outbreak ended
The full story
The cruise ship hantavirus outbreak ended
The WHO declared the hantavirus outbreak linked to the cruise ship MV Hondius over on 2 July.
Why it matters. The WHO is now running a study in 21 countries on how the disease develops, to help build tests, drugs and vaccines for future outbreaks.
US addiction grants cut, then restored
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On 13 January, SAMHSA, the US federal agency for mental health and addiction, cancelled hundreds of grants worth about $2 billion.
After protests from both parties, the money was restored the next evening.
Why it matters
Medicaid, the US government's health insurance for people on low incomes, pays for a quarter of US spending on mental health and addiction care.
Why it matters
The 2025 budget law cuts its federal funding by $1 trillion over 10 years.
The full story
US addiction grants cut, then restored
On 13 January, SAMHSA, the US federal agency for mental health and addiction, cancelled hundreds of grants worth about $2 billion.
Why it matters. Medicaid, the US government's health insurance for people on low incomes, pays for a quarter of US spending on mental health and addiction care. The 2025 budget law cuts its federal funding by $1 trillion over 10 years.
Britain's new clinical trial rules
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The UK's biggest change to its rules for medicine trials in more than 20 years came into force on 28 April.
The Health Research Authority and the Medicines and Healthcare products Regulatory Agency, the UK drug regulator, wrote them together.
They line up how the regulator and ethics committees review applications, and aim to speed approvals while protecting volunteers.
Why it matters
Every new medicine reaches patients only after trials, so these rules set how fast UK trials can start and how volunteers are protected.
Why it matters
The law was signed in April 2025 and given a year to take effect.
The full story
Britain's new clinical trial rules
The UK's biggest change to its rules for medicine trials in more than 20 years came into force on 28 April.
Why it matters. Every new medicine reaches patients only after trials, so these rules set how fast UK trials can start and how volunteers are protected. The law was signed in April 2025 and given a year to take effect.
Few medical AI tools tested properly
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A review published this year in npj Digital Medicine sorted 4,667 studies of medical AI.
88.2% were early lab-stage work, and only 2.4%, or 113 studies, were randomised trials in patients.
82.3% reported good results, but many had weak methods.
Why it matters
The research came mostly from a few countries: ten produced three quarters of it.
Why it matters
Only a trial shows whether a tool helps patients, and fewer than one study in 40 was one.
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Few medical AI tools tested properly
The full story
Few medical AI tools tested properly
A review published this year in npj Digital Medicine sorted 4,667 studies of medical AI.
Why it matters. The research came mostly from a few countries: ten produced three quarters of it.
The truth, across the day
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Why it works on people
A vaccine with a well-known name sounds like a solution, and the name does not say which virus it was built for.
That's the whole Mind & body day.
35 stories, 49 sources.