Sunday, 25 October 2026
Sunday, 25 October 2026
- In brief
- 1Amgen's Imdelltra added to Imfinzi cuts the risk of death by 58% in small cell lung cancer, in a final trial shown at ESMO
- 2AstraZeneca's bladder pair trails a rival
- 3Bayer's Nubeqa holds back prostate cancer
- 4Erleada before and after prostate surgery
- 5The melanoma vaccine is shown in Madrid
- 6Novartis's MS pill falls short of hopes
- 7Lilly's ovarian cancer drug shrinks most tumours
- 8A drug pair without chemotherapy for pancreatic cancer
- 9Dr Reddy's swaps in new Ozempic copies
- 10UK approves a daily pill for psoriasis
- 11US measles cases reach 4,588
- 12Nigeria's Ebola case linked to Kenya's
- 13A baby dies of mpox in Karachi
- 14Uganda runs short of a twice-yearly HIV jab
- 15AstraZeneca puts $50m into Abu Dhabi trials
- 16An ear device for stubborn blood pressure
- 17Boehringer's rival drug tried in rarer cancers
- 18China nearly matches India on malaria drugs for Africa
25 Oct · Biotech · In brief
Biotech · Sunday, 25 October 2026
Biotech, in brief
18 stories · 23 sources
Swipe up for the day in brief ↑Scroll down for the day in brief ↓
What is moving · 1 of 4
Cancer drugs moved earlier
Amgen tested Imdelltra straight after patients' first treatment, not after it had failed.
What is moving · 2 of 4
Judged against a rival
AstraZeneca's bladder cancer pair beat surgery alone but fell short of Merck's Keytruda with Padcev.
What is moving · 3 of 4
Germs spreading
US measles cases rose by 178 in a week to 4,588.
What is moving · 4 of 4
Medicines running short
Dr Reddy's, an Indian drugmaker, stopped supplying its first copy of Ozempic in July after finding an impurity.
11 sources
Biotech, in brief
- 3ESMO 2026 news: The ESMO presentation everyone's been waiting for
- 4Amgen says drug combo cuts risk of death by 58% in patients with aggressive lung cancer
- 6ESMO 2026: Nubeqa (darolutamide) plus ADT and radiation therapy reduces risk of metastasis or death by 58% in prostate cancer patients at high risk of recurrence
- 7Johnson & Johnson announces Erleada (apalutamide) treatment before and after surgery reduces risk of recurrence or death by 62% versus surgery alone in high-risk prostate cancer
- 9Novartis MS pill falls short of analyst expectations in late-stage trials
- 12ESMO: Lilly ADC sees 79% ORR in competitive ovarian cancer space
- 14Dr Reddy's rolls out new generic Ozempic brands to ease Obeda supply hit
- 17Additional 178 cases of measles reported by US health authorities amid outbreak
- 18Woman, 65, becomes second patient to die of Ebola in Kenya
- 19First infant battling mpox dies in Karachi hospital
- 20HIV prevention jab offers hope in Uganda but doses are hard to find
Amgen's Imdelltra added to Imfinzi cuts the risk of death by 58% in small cell lung cancer, in a final trial shown at ESMO
Swipe up for the story ↑Scroll down for the story ↓
Amgen, a US drugmaker, said on Saturday that adding its immune drug Imdelltra to AstraZeneca's immune drug Imfinzi cut the risk of death by 58% in extensive-stage small cell lung cancer.
only one case was severe, and none was life-threatening
Who is involved
Amgen
a large US drugmaker; it makes Imdelltra and ran the trial
Who is involved
AstraZeneca
a British-Swedish drugmaker; it makes Imfinzi and paid for part of the trial
Why it matters
The next step is the drug regulators: Amgen says it is sharing the results with them worldwide, and the 21-month figure will change as patients are followed for longer.
What's really going on
At ESMO in Madrid, Amgen showed that adding its drug Imdelltra to AstraZeneca's Imfinzi kept more people with a fast lung cancer alive, so both companies stand to sell their drug to more patients for longer.
Why it works on people
One large percentage such as 58% sounds like a share of patients saved, when it is a comparison of risk between two groups.
Who gains
Amgen
Imdelltra is now approved only after chemotherapy fails, and a survival gain at the start of treatment could widen its use beyond the $627 million it sold in 2025.
Who gains
AstraZeneca
Its Imfinzi is given in both groups of the trial, so every patient who gets the new pair still takes Imfinzi.
Who pays
Patients given the Imdelltra pair
Half had an immune overreaction, serious side effects doubled from 10.8% to 20.9%, and each must be watched in a clinic for hours after the first two doses.
Nobody knows yet
How long the Imdelltra pair really keeps people alive.
The 21.1 months comes from a planned early look at about 16 months of follow-up, and the trial's leader says the figure may change as patients are followed for longer.
Nobody knows yet
Whether the pair beats other ways of starting treatment.
The trial compared it only with Imfinzi alone, so no result exists against other first treatments.
Good news
In a final trial of people with small cell lung cancer that had spread, 79 in every 100 given Amgen's Imdelltra with Imfinzi were alive a year later, against 53 on Imfinzi alone.
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
Jacob Sands
a lung cancer doctor at Dana-Farber Cancer Institute in Boston; he led the trial and presented it
Part 1 of 13 · Who else is involved
Stephen Liu
a cancer doctor at Georgetown University who reviewed the trial at the meeting; he said he would offer it to every eligible group
Part 2 of 13 · How it unfolded
Before
Imdelltra is approved only after chemotherapy has failed
DeLLphi-304
given later in the illness, half lived 13.6 months on it against 8.4 on chemotherapy
Part 3 of 13
Small cell lung cancer grows fast, and extensive-stage means it has already spread beyond the lung where it began.
Part 4 of 13
The DeLLphi-305 trial had 563 patients whose cancer had not grown after a first round of Imfinzi with chemotherapy.
Part 5 of 13
Half then got Imdelltra with Imfinzi, and half got Imfinzi alone, as maintenance: treatment kept up after the first heavy round.
Part 6 of 13
Half the patients on the pair were still alive at 21.1 months, against 12.7 months on Imfinzi alone.
Part 7 of 13
After one year, 79% of patients on the pair were alive, against 53% on Imfinzi alone.
Part 8 of 13
Imdelltra grabs a protein called DLL3 on cancer cells and a protein on T cells, the immune cells that kill, and pulls the two together.
Part 9 of 13
Almost half the patients on Imdelltra had cytokine release syndrome, an immune overreaction, though nearly every case was mild or moderate.
Part 10 of 13
Serious side effects linked to treatment hit 20.9% of patients on the pair and 10.8% on Imfinzi alone.
Part 11 of 13
Imdelltra is now approved only for patients whose cancer grew during or after platinum chemotherapy, and it sold $627 million in 2025.
Part 12 of 13
The trial compared the pair only with Imfinzi alone, not with other ways of starting treatment.
Part 13 of 13
The results were shown at ESMO, Europe's biggest cancer meeting, in Madrid, and published the same day in the New England Journal of Medicine.
4 sources
Amgen's Imdelltra added to Imfinzi cuts the risk of death by 58% in small cell lung cancer, in a final trial shown at ESMO
- 1Imdelltra in combination with Imfinzi reduced risk of death by an unprecedented 58% in first-line extensive stage small cell lung cancer
- 2Imfinzi (durvalumab) plus tarlatamab-dlle reduced the risk of death by 58% in 1st-line extensive-stage small cell lung cancer in the DeLLphi-305 Phase III trial
- 3ESMO 2026 news: The ESMO presentation everyone's been waiting for
- 4Amgen says drug combo cuts risk of death by 58% in patients with aggressive lung cancer
The full story
Amgen's Imdelltra added to Imfinzi cuts the risk of death by 58% in small cell lung cancer, in a final trial shown at ESMO
Amgen, a US drugmaker, said on Saturday that adding its immune drug Imdelltra to AstraZeneca's immune drug Imfinzi cut the risk of death by 58% in extensive-stage small cell lung cancer.
Small cell lung cancer grows fast, and extensive-stage means it has already spread beyond the lung where it began.
The DeLLphi-305 trial had 563 patients whose cancer had not grown after a first round of Imfinzi with chemotherapy.
Half then got Imdelltra with Imfinzi, and half got Imfinzi alone, as maintenance: treatment kept up after the first heavy round.
Half the patients on the pair were still alive at 21.1 months, against 12.7 months on Imfinzi alone.
After one year, 79% of patients on the pair were alive, against 53% on Imfinzi alone.
Imdelltra grabs a protein called DLL3 on cancer cells and a protein on T cells, the immune cells that kill, and pulls the two together.
Almost half the patients on Imdelltra had cytokine release syndrome, an immune overreaction, though nearly every case was mild or moderate.
Serious side effects linked to treatment hit 20.9% of patients on the pair and 10.8% on Imfinzi alone.
Imdelltra is now approved only for patients whose cancer grew during or after platinum chemotherapy, and it sold $627 million in 2025.
The trial compared the pair only with Imfinzi alone, not with other ways of starting treatment.
The results were shown at ESMO, Europe's biggest cancer meeting, in Madrid, and published the same day in the New England Journal of Medicine.
Why it matters. The next step is the drug regulators: Amgen says it is sharing the results with them worldwide, and the 21-month figure will change as patients are followed for longer.
AstraZeneca's bladder pair trails a rival
Swipe up for the story ↑Scroll down for the story ↓
AstraZeneca showed final-trial results at ESMO for its immune drug Imfinzi, given with Pfizer's drug Padcev before bladder surgery and alone after it.
The VOLGA trial was in muscle-invasive bladder cancer, which has grown into the bladder wall.
After two years, 78% of patients on it were alive, against 69% after surgery alone.
Why it matters
Merck's Keytruda with Padcev, already the standard before surgery, cut the risk of death by 50% in its own trial, so STAT reports that AstraZeneca's pair falls short.
Why it matters
The two figures come from separate trials with different patients.
How it works
Why the same 58% cut in risk can mean very different gains for patients
How it works
A "58% lower risk" compares two groups, so it cannot say alone how many people it helps: that depends on how many would have died anyway.
How it works · step 1 of 6
A trial splits patients into two groups and counts deaths in each
How it works · step 2 of 6
The headline compares the two groups' risks as a ratio, such as 0.42
How it works · step 3 of 6
A ratio of 0.42 is reported as a 58% lower risk
How it works · step 4 of 6
Where many in the comparison group die, 58% of their risk is many lives
How it works · step 5 of 6
Where few would die anyway, the same 58% is a handful
How it works · step 6 of 6
So the real gain shows only in each group's own numbers: months, or people per 100
The twist
A 58% lower risk does not mean 58 people in 100 are helped.
The twist
In the lung trial it meant 26 more people in 100 alive after a year, and in the prostate trial 7 more men in 100 free of spread after four years.
The picture
Both trials reported a 58% lower risk. Compare each pair of bars: 26 people in 100 in the lung trial, 7 in 100 in the prostate trial.
Seen the same day
A 62% lower risk of the cancer returning became 63 against 41 men in 100 free of it after three years, about 22 more.
Seen the same day
A 42% lower risk of death became 78 against 69 people in 100 alive after two years, 9 more.
Seen the same day
A 35% cut in the yearly relapse rate was turned by the presenting doctor into about one relapse every 13 years.
Seen the same day
The same 58% as the lung trial meant 95 against 88 men in 100 free of spread, because few men in either group had the cancer spread.
The catch
The ratio is still useful, because it often stays similar from one group of patients to another, while the gain in people per 100 changes with how sick the group is.
The whole
A patient wants to know their own chance, a health service the cost of each extra year, and an investor the sales.
The whole
All three start from the same 58%, and none of them can get an answer from it alone.
What's really going on
Most of the day's other cancer results were measured against surgery alone, a dummy pill or an older drug, and two of them fell short of a rival's own trial.
Who gains
Merck
Its Keytruda with Padcev, the standard before bladder surgery, cut the risk of death by 50% in its own trial, against 42% for AstraZeneca's pair in a separate one.
4 sources
AstraZeneca's bladder pair trails a rival
- 3ESMO 2026 news: The ESMO presentation everyone's been waiting for
- 6ESMO 2026: Nubeqa (darolutamide) plus ADT and radiation therapy reduces risk of metastasis or death by 58% in prostate cancer patients at high risk of recurrence
- 7Johnson & Johnson announces Erleada (apalutamide) treatment before and after surgery reduces risk of recurrence or death by 62% versus surgery alone in high-risk prostate cancer
- 9Novartis MS pill falls short of analyst expectations in late-stage trials
The full story
AstraZeneca's bladder pair trails a rival
AstraZeneca showed final-trial results at ESMO for its immune drug Imfinzi, given with Pfizer's drug Padcev before bladder surgery and alone after it.
Why it matters. Merck's Keytruda with Padcev, already the standard before surgery, cut the risk of death by 50% in its own trial, so STAT reports that AstraZeneca's pair falls short.
Bayer's Nubeqa holds back prostate cancer
Swipe up for the story ↑Scroll down for the story ↓
Bayer said adding its pill Nubeqa to hormone treatment and radiation cut the risk of prostate cancer spreading, or death, by 58%.
The DASL-HiCaP trial, run by researchers rather than the company, had 1,106 men whose cancer was at high risk of coming back.
After four years, 95% on Nubeqa were free of spread, against 88% on a dummy pill.
Why it matters
After four years, 97% of men on Nubeqa and 95% on the dummy pill are alive, and the doctors are still following them.
Why it matters
The trial's 58% matches the lung trial's figure, but here it stands for 7 more men in 100 free of spread.
How it works
The same 58% as the lung trial meant 95 against 88 men in 100 free of spread, because few men in either group had the cancer spread.
The idea, in story 2: Why the same 58% cut in risk can mean very different gains for patients →Nobody knows yet
Whether Nubeqa and Erleada lengthen men's lives.
After four years, 97% of men on Nubeqa and 95% on the dummy pill are alive, and both companies say follow-up for survival goes on.
Good news
Among 1,106 men with prostate cancer at high risk of coming back, 95 in 100 given Bayer's Nubeqa with radiation were free of spread four years later.
2 sources
Bayer's Nubeqa holds back prostate cancer
- 6ESMO 2026: Nubeqa (darolutamide) plus ADT and radiation therapy reduces risk of metastasis or death by 58% in prostate cancer patients at high risk of recurrence
- 7Johnson & Johnson announces Erleada (apalutamide) treatment before and after surgery reduces risk of recurrence or death by 62% versus surgery alone in high-risk prostate cancer
The full story
Bayer's Nubeqa holds back prostate cancer
Bayer said adding its pill Nubeqa to hormone treatment and radiation cut the risk of prostate cancer spreading, or death, by 58%.
Why it matters. After four years, 97% of men on Nubeqa and 95% on the dummy pill are alive, and the doctors are still following them.
Erleada before and after prostate surgery
Swipe up for the story ↑Scroll down for the story ↓
Johnson & Johnson said its pill Erleada, given with hormone treatment before and after surgery, cut the risk of prostate cancer returning, or death, by 62% against surgery alone.
The trial had 408 men with high-risk cancer that had not spread, followed for a median 37.8 months.
After three years, 63% on the drugs had no sign of the cancer returning, against 41.4% after surgery alone.
Why it matters
Serious side effects were more common on the drugs, 31% against 22%, and 64% of men had hot flushes.
Why it matters
Erleada is not approved for this use, and nobody yet knows whether the men will live longer.
How it works
A 62% lower risk of the cancer returning became 63 against 41 men in 100 free of it after three years, about 22 more.
The idea, in story 2: Why the same 58% cut in risk can mean very different gains for patients →Who pays
Men given Erleada around surgery
Serious side effects rose from 22% to 31%, and 64% had hot flushes.
1 source
Erleada before and after prostate surgery
The full story
Erleada before and after prostate surgery
Johnson & Johnson said its pill Erleada, given with hormone treatment before and after surgery, cut the risk of prostate cancer returning, or death, by 62% against surgery alone.
Why it matters. Serious side effects were more common on the drugs, 31% against 22%, and 64% of men had hot flushes.
The melanoma vaccine is shown in Madrid
Swipe up for the story ↑Scroll down for the story ↓
Georgina Long of the Melanoma Institute Australia presented the trial of intismeran, a vaccine made for each patient by Moderna and Merck, at ESMO on Saturday.
Its results had leaked two days earlier: added to Merck's Keytruda, it cut the risk of melanoma, a skin cancer, returning or death by 42%.
The cut in the risk of the cancer spreading to distant organs, 38%, was smaller than an earlier trial had led people to expect.
Why it matters
Inge Marie Svane of the University of Copenhagen, who reviewed the trial at the meeting, said it is not yet known whether the vaccine helps people live longer.
Why it matters
Merck hopes for US approval next year, and the full results appear in a journal next month.
Nobody knows yet
Whether the melanoma vaccine helps people live longer.
The trial measured the cancer returning, and the doctor who reviewed it at ESMO said a survival benefit is not yet known.
2 sources
The melanoma vaccine is shown in Madrid
The full story
The melanoma vaccine is shown in Madrid
Georgina Long of the Melanoma Institute Australia presented the trial of intismeran, a vaccine made for each patient by Moderna and Merck, at ESMO on Saturday.
Why it matters. Inge Marie Svane of the University of Copenhagen, who reviewed the trial at the meeting, said it is not yet known whether the vaccine helps people live longer.
Novartis's MS pill falls short of hopes
Swipe up for the story ↑Scroll down for the story ↓
Novartis said its pill remibrutinib cut the yearly rate of multiple sclerosis relapses by 35% and 31% in two final trials, against Sanofi's older drug Aubagio.
In multiple sclerosis the immune system damages nerves, and a relapse is a flare of symptoms.
Analysts at BNP Paribas had expected about 50%, and Reuters puts analysts' hopes at 45% to 60%.
Roche's rival drug fenebrutinib cut relapses by 51% and 59% in its own trials.
Why it matters
Heinz Wiendl, the neurologist who presented the data, said the rate on remibrutinib works out at about one relapse every 13 years.
Why it matters
STAT reports that its safety record is cleaner, which could still help it compete.
How it works
A 35% cut in the yearly relapse rate was turned by the presenting doctor into about one relapse every 13 years.
The idea, in story 2: Why the same 58% cut in risk can mean very different gains for patients →Who gains
Roche
Novartis's pill prevented fewer relapses than expected, which Bloomberg says may give Roche's rival fenebrutinib an advantage.
Nobody knows yet
Whether remibrutinib's cleaner safety makes up for fewer relapses prevented.
Novartis and Roche tested their drugs in separate trials against Aubagio, and no trial has put the two side by side.
The full story
Novartis's MS pill falls short of hopes
Novartis said its pill remibrutinib cut the yearly rate of multiple sclerosis relapses by 35% and 31% in two final trials, against Sanofi's older drug Aubagio.
Why it matters. Heinz Wiendl, the neurologist who presented the data, said the rate on remibrutinib works out at about one relapse every 13 years.
Lilly's ovarian cancer drug shrinks most tumours
Swipe up for the story ↑Scroll down for the story ↓
Eli Lilly showed early results at ESMO for sofetabart mipitecan, a drug that carries a cell-killing poison to cancer cells bearing a protein called FRa.
In 33 women whose ovarian cancer came back at least six months after platinum chemotherapy, given it with the drug bevacizumab, tumours shrank in 79.3%.
In 20.7%, scans found no cancer left.
Why it matters
AbbVie, Genmab and AstraZeneca have rival drugs aimed at the same protein, and Lilly began its final trial a year ago.
Why it matters
Patients may grow resistant to the poison most of the new drugs share, so Fierce Biotech says being first to market could matter more.
1 source
Lilly's ovarian cancer drug shrinks most tumours
The full story
Lilly's ovarian cancer drug shrinks most tumours
Eli Lilly showed early results at ESMO for sofetabart mipitecan, a drug that carries a cell-killing poison to cancer cells bearing a protein called FRa.
Why it matters. AbbVie, Genmab and AstraZeneca have rival drugs aimed at the same protein, and Lilly began its final trial a year ago.
A drug pair without chemotherapy for pancreatic cancer
Swipe up for the story ↑Scroll down for the story ↓
An experimental drug from Tango Therapeutics, given with Revolution Medicines' approved pill Rasonque, shrank tumours in 82% of patients with one kind of advanced pancreatic cancer, results shown on Friday at ESMO.
After nine months, 88% were alive with no tumour growth.
Why it matters
STAT says the result backs the idea that pancreatic cancer patients gain more from pairs of targeted drugs than from one.
Nobody knows yet
How many people were in Tango's pancreatic cancer trial.
The 82% and 88% figures come from the opening of a report whose full text is for subscribers, and the patient count was not in it.
1 source
A drug pair without chemotherapy for pancreatic cancer
The full story
A drug pair without chemotherapy for pancreatic cancer
An experimental drug from Tango Therapeutics, given with Revolution Medicines' approved pill Rasonque, shrank tumours in 82% of patients with one kind of advanced pancreatic cancer, results shown on Friday at ESMO.
Why it matters. STAT says the result backs the idea that pancreatic cancer patients gain more from pairs of targeted drugs than from one.
Dr Reddy's swaps in new Ozempic copies
Swipe up for the story ↑Scroll down for the story ↓
Dr Reddy's Laboratories, an Indian maker of cheaper copies of drugs, has started selling two new brands of semaglutide, the active ingredient in Novo Nordisk's Ozempic and Wegovy, Reuters reported.
Supplies of its first brand, Obeda, stopped in July after it found an impurity in the ingredient.
The new brands, Obeda Pro and Obeda Plus, are made by another company, Hetero Labs.
Why it matters
Dr Reddy's launched Obeda in India in March, after semaglutide lost its patent there, and a race among Indian drugmakers followed.
Why it matters
It says Obeda returns next month in India and this quarter in Canada.
Who gains
Hetero Labs
It makes Dr Reddy's two new semaglutide brands, which filled the gap left when the first brand was halted.
Who pays
Dr Reddy's
The semaglutide recall in Canada cost it 710 million rupees of sales in its latest quarter.
2 sources
Dr Reddy's swaps in new Ozempic copies
The full story
Dr Reddy's swaps in new Ozempic copies
Dr Reddy's Laboratories, an Indian maker of cheaper copies of drugs, has started selling two new brands of semaglutide, the active ingredient in Novo Nordisk's Ozempic and Wegovy, Reuters reported.
Why it matters. Dr Reddy's launched Obeda in India in March, after semaglutide lost its patent there, and a race among Indian drugmakers followed.
UK approves a daily pill for psoriasis
Swipe up for the story ↑Scroll down for the story ↓
The MHRA, Britain's medicines regulator, approved Johnson & Johnson's daily pill Icotyde on Friday for moderate to severe plaque psoriasis.
Plaque psoriasis is a skin condition that causes red, scaly and often itchy or painful patches.
The approval covers adults and children aged 12 and over who weigh at least 40kg.
It rests on four final trials in 2,500 people, in which the pill beat a dummy pill after 16 weeks.
Why it matters
The US approved Icotyde earlier this year, and J&J, which makes it with Protagonist Therapeutics, expects $5 billion a year in peak sales.
Why it matters
It is also being tested in ulcerative colitis, psoriatic arthritis and Crohn's disease.
Good news
Britain approved Johnson & Johnson's daily pill Icotyde for plaque psoriasis, for adults and for children aged 12 and over.
The full story
UK approves a daily pill for psoriasis
The MHRA, Britain's medicines regulator, approved Johnson & Johnson's daily pill Icotyde on Friday for moderate to severe plaque psoriasis.
Why it matters. The US approved Icotyde earlier this year, and J&J, which makes it with Protagonist Therapeutics, expects $5 billion a year in peak sales.
US measles cases reach 4,588
Swipe up for the story ↑Scroll down for the story ↓
The CDC, the US national public health agency, reported 178 more measles cases this week, taking the 2026 total to 4,588 as of Friday.
That is more than double last year's total, across at least 43 outbreaks.
The CDC counts three measles deaths nationally, while Pennsylvania reports five and is looking into a sixth.
Why it matters
The measles vaccine prevents 97% of cases, and one in five unvaccinated people who catch measles ends up in hospital.
Why it matters
The US health department also proposed this week to let doctors bill for reporting suspected vaccine injuries.
Nobody knows yet
How many people have died of measles in the US this year.
The CDC counts three deaths and will not say where the third was, while Pennsylvania alone reports five.
1 source
US measles cases reach 4,588
The full story
US measles cases reach 4,588
The CDC, the US national public health agency, reported 178 more measles cases this week, taking the 2026 total to 4,588 as of Friday.
Why it matters. The measles vaccine prevents 97% of cases, and one in five unvaccinated people who catch measles ends up in hospital.
Nigeria's Ebola case linked to Kenya's
Swipe up for the story ↑Scroll down for the story ↓
Ali Pate, Nigeria's health minister, said the country's only confirmed Ebola case appears genetically related to a strain found earlier in Kenya.
He said there is no evidence yet that the Kenyan patient went to Nigeria, and more tests are under way.
Both patients are believed to have passed through Entebbe airport in Uganda this month.
Uganda said on Friday that people who have been to DR Congo can no longer change planes there.
Why it matters
The outbreak began in DR Congo in May and has more than 9,500 cases there and over 4,000 deaths across Africa.
Why it matters
It is caused by the Bundibugyo kind of Ebola, which has no approved vaccine or treatment.
Nobody knows yet
How Nigeria's Ebola patient was infected.
Her virus appears related to a strain found in Kenya, but there is no evidence the Kenyan patient went to Nigeria and tests continue.
1 source
Nigeria's Ebola case linked to Kenya's
The full story
Nigeria's Ebola case linked to Kenya's
Ali Pate, Nigeria's health minister, said the country's only confirmed Ebola case appears genetically related to a strain found earlier in Kenya.
Why it matters. The outbreak began in DR Congo in May and has more than 9,500 cases there and over 4,000 deaths across Africa.
A baby dies of mpox in Karachi
Swipe up for the story ↑Scroll down for the story ↓
A 52-day-old boy died of mpox early on Saturday at a Karachi hospital, the first baby to die of it in the Pakistani city, Dawn reported.
Dawn's sources say he caught it during a circumcision at a hospital in Malir that officials have since sealed.
12 of 98
mpox deaths among cases in Sindh this year
Mpox is a virus that causes a rash and spreads through close contact and shared objects.
Why it matters
Nearly all who died were babies infected in clinics without proper infection control, Dawn's sources said.
Who pays
Families of babies in Sindh
Nearly all of the province's 12 mpox deaths this year were babies infected in clinics without proper infection control.
The full story
A baby dies of mpox in Karachi
A 52-day-old boy died of mpox early on Saturday at a Karachi hospital, the first baby to die of it in the Pakistani city, Dawn reported.
12 of 98
mpox deaths among cases in Sindh this year
Why it matters. Nearly all who died were babies infected in clinics without proper infection control, Dawn's sources said.
Uganda runs short of a twice-yearly HIV jab
Swipe up for the story ↑Scroll down for the story ↓
Lenacapavir, a jab given every six months that nearly stopped new HIV infections in two big trials, is often unavailable in Mbarara, a city in western Uganda, africanews reported.
Uganda has rationed a few thousand doses across the country, so many people get a two-monthly jab, cabotegravir, instead.
The founder of a local HIV group says funding cuts ended outreach that used to test people.
Why it matters
The Global Fund, which pays for HIV drugs in poorer countries, says 430,000 doses had been delivered by mid-September.
Why it matters
Gilead, which makes lenacapavir, says it supplies it at no profit while licensed makers of cheaper copies scale up.
Who pays
People seeking HIV protection in Mbarara
Lenacapavir is often finished when they ask for it, so many take a jab every two months instead of every six.
Good news
By mid-September, national programmes reported more than 118,000 people receiving lenacapavir, a jab given twice a year that nearly stopped new HIV infections in two big trials.
1 source
Uganda runs short of a twice-yearly HIV jab
The full story
Uganda runs short of a twice-yearly HIV jab
Lenacapavir, a jab given every six months that nearly stopped new HIV infections in two big trials, is often unavailable in Mbarara, a city in western Uganda, africanews reported.
Why it matters. The Global Fund, which pays for HIV drugs in poorer countries, says 430,000 doses had been delivered by mid-September.
AstraZeneca puts $50m into Abu Dhabi trials
Swipe up for the story ↑Scroll down for the story ↓
AstraZeneca will spend about $50 million over the next few years on roughly 30 clinical trials in Abu Dhabi, with Cleveland Clinic Abu Dhabi, a hospital there.
The trials will study heart, kidney and metabolic diseases, and the first should start before the end of this year.
Heart disease causes 34% of deaths in the UAE, its health ministry says.
AstraZeneca also announced a project with Oracle to use AI and health records to find high blood pressure earlier.
Why it matters
Iskra Reic of AstraZeneca said the UAE suits such work because its medical records are well connected and it holds Emirati genetic data.
Why it matters
She said more patients there could join global trials.
1 source
AstraZeneca puts $50m into Abu Dhabi trials
The full story
AstraZeneca puts $50m into Abu Dhabi trials
AstraZeneca will spend about $50 million over the next few years on roughly 30 clinical trials in Abu Dhabi, with Cleveland Clinic Abu Dhabi, a hospital there.
Why it matters. Iskra Reic of AstraZeneca said the UAE suits such work because its medical records are well connected and it holds Emirati genetic data.
An ear device for stubborn blood pressure
Swipe up for the story ↑Scroll down for the story ↓
Researchers at Queen Mary University of London tested a small device that sends gentle electrical pulses into nerves in the ear, in 63 people whose blood pressure stayed high despite medicine.
Half used the real device and half a fake one, at home, for 12 weeks.
In people with more severe high blood pressure, a group chosen before the trial began, it fell more.
Why it matters
The device was safe and most people used it as told, but the trial was small.
1 source
An ear device for stubborn blood pressure
The full story
An ear device for stubborn blood pressure
Researchers at Queen Mary University of London tested a small device that sends gentle electrical pulses into nerves in the ear, in 63 people whose blood pressure stayed high despite medicine.
Why it matters. The device was safe and most people used it as told, but the trial was small.
Boehringer's rival drug tried in rarer cancers
Swipe up for the story ↑Scroll down for the story ↓
Boehringer Ingelheim, a German drugmaker, showed early results at ESMO for obrixtamig, which, like Imdelltra, links immune cells to the DLL3 protein on cancer cells.
In neuroendocrine cancers outside the lung, given with platinum chemotherapy as a first treatment, tumours were held back for a median 7.7 months.
This year Boehringer began two final trials: one in people starting treatment for small cell lung cancer, and one in these rarer cancers.
Why it matters
Boehringer's lung trial pairs obrixtamig with Roche's immune drug Tecentriq at the start of treatment, the stage where Amgen has now shown a survival gain.
2 sources
Boehringer's rival drug tried in rarer cancers
The full story
Boehringer's rival drug tried in rarer cancers
Boehringer Ingelheim, a German drugmaker, showed early results at ESMO for obrixtamig, which, like Imdelltra, links immune cells to the DLL3 protein on cancer cells.
Why it matters. Boehringer's lung trial pairs obrixtamig with Roche's immune drug Tecentriq at the start of treatment, the stage where Amgen has now shown a survival gain.
China nearly matches India on malaria drugs for Africa
Swipe up for the story ↑Scroll down for the story ↓
China's exports of malaria drugs to 12 of the African countries worst hit by the disease reached $89.3 million last year, a new study found.
India's reached $89.6 million, so the two are now almost level, according to Sol Gravitas, an Indian market research firm.
In 2021, India sold $121 million of these drugs to the same countries and China $62.6 million.
Malaria is a disease spread by mosquito bites, and most of its cases are in Africa.
Why it matters
Indian drugmakers have long been the main suppliers of malaria medicines in these countries, and Chinese firms closed almost all of the gap in four years.
Why it matters
The figures cover only these 12 countries and come from one research firm.
1 source
China nearly matches India on malaria drugs for Africa
The full story
China nearly matches India on malaria drugs for Africa
China's exports of malaria drugs to 12 of the African countries worst hit by the disease reached $89.3 million last year, a new study found.
Why it matters. Indian drugmakers have long been the main suppliers of malaria medicines in these countries, and Chinese firms closed almost all of the gap in four years.
That's the whole Biotech day.
18 stories, 23 sources.