| UPDATED: iTeos-GSK's TIGIT combo shows 30% more tumor shrinkage than Jemperli, but safety signals scare investors
Bristol Myers moves Opdualag into phase 3 trials in competitive first-line lung cancer field
'Cooking with gas': Regeneron sees its Opdualag rival as next big thing for treating solid tumors
Pfizer sees weight gain in cancer patients, aims to enter phase 3 in 2025
Despite checkered past, Merck's Keytruda-Lenvima pairing looks to change practice in liver cancer subtype
AstraZeneca steps out from Daiichi's shadow, posting data on ADC rivals to AbbVie, Pfizer
AstraZeneca's Imfinzi extends life in bladder cancer type. Will FDA push back on its perioperative trial design?
AstraZeneca stands by Truqap despite surprise breast cancer flop
Merck unpacks a mixed bag of gynecological cancer results for Keytruda
IO Biotech's vaccine and Keytruda combo hits primary endpoint in phase 2 squamous cell carcinoma trial
Bristol Myers axes Immatics' bispecific after $150M bet
GSK's Zejula misses survival goal in first-line ovarian cancer, as pharma&'s combo disappoints
Even after unique trial win, Incyte CEO views PD-1 drug Zynyz as pipeline aide
Lantheus' phase 3 radiotherapy readout not enough to topple Pluvicto, say analysts
With survival win, Merck's Keytruda redeems itself in early triple-negative breast cancer
Despite survival miss, Exelixis presses on with FDA prostate cancer bid as Ipsen scraps EU plan
Bayer hopes to expand Nubeqa's prostate cancer reach with chemo-free regimen
Despite positive trial, Merck's Welireg still comes up short in overall survival
Jazz HER2 bispecific posts 59% survival at 30 months in gastric cancer
AZ, Daiichi build case for Enhertu in breast cancer patients with brain metastases
Exact Sciences shows off early colorectal cancer blood test data |
| By Gabrielle Masson After announcing a phase 3 launch based on positive midstage results, iTeos and GSK are finally sharing the highlights from the phase 2 TIGIT trial, revealing a more than 30% difference in confirmed overall response rates between the investigational treatment versus monotherapy. |
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By Angus Liu More than two years after an initial FDA approval in melanoma, Bristol Myers Squibb is moving its PD-1/LAG-3 combo Opdualag into registrational testing in one of the most important disease areas—first-line non-small cell lung cancer. |
By Gabrielle Masson Regeneron is back with long-term follow-up results for its LAG-3 inhibitor and PD-1 inhibitor combo in advanced melanoma, phase 1 findings that have prompted the company to launch four phase 3 programs with the intent to rival Bristol Myers Squibb's Opdualag. |
By Nick Paul Taylor Cancer patients with wasting syndrome have gained weight after taking Pfizer’s anti-GDF-15 antibody in a midphase study, emboldening the Big Pharma to target a 2025 start date for its pivotal trial program. |
By Angus Liu After a surprise failure in advanced liver cancer, Merck & Co. and Eisai are hoping new data can make their Keytruda-Lenvima combination a standard of care in intermediate-stage disease. But questions remain. |
By Nick Paul Taylor AstraZeneca has shared an early look at the performance of its in-house antibody-drug conjugate technology, publishing phase 1 data on candidates that could compete with molecules from AbbVie and Pfizer. |
By Angus Liu AstraZeneca’s detailed data show exactly how Imfinzi became the first PD-1/L1 inhibitor to deliver a patient survival win in muscle-invasive bladder cancer. But the win came from a perioperative regimen, a trial design that’s been criticized by the FDA in lung cancer. |
By Angus Liu AstraZeneca is detailing Truqap's pivotal trial flop in triple-negative breast cancer, a result that could raise additional doubts around the first-in-class AKT inhibitor. From AZ's perspective, a company executive argued the failure was probably a one-off. |
By Zoey Becker The company unveiled new data from its KEYNOTE-A18 study in late stage cervical cancer and its failed KEYNOTE-B21 trial testing Keytruda as an adjuvant therapy in newly diagnosed endometrial cancer. |
By Darren Incorvaia Immune checkpoint inhibitors are the superheroes of cancer therapy. Drugs like Bristol Myers Squibb’s Opdivo and Merck’s Keytruda are among the most profitable in the world—Keytruda pulled in $25 billion last year, making it the bestselling drug of 2023. But every good superhero needs a sidekick. |
By Nick Paul Taylor Bristol Myers Squibb has jettisoned another cancer candidate in-licensed under its former CEO. Immatics is the latest partner to get a termination notice, leaving it in full control of a bispecific molecule that BMS picked up for $150 million upfront late in 2021. |
By Angus Liu In a rough day for PARP inhibitors in ovarian cancer, GSK’s Zejula didn’t deliver a life extension benefit in the final analysis of a phase 3 trial. Another study showed that pharma&’s attempt to enhance its Rubraca with Bristol Myers Squibb’s Opdivo seriously backfired. |
By Angus Liu Incyte’s late PD-1 entrant Zynyz has chalked up a unique clinical win. Yet company CEO Hervé Hoppenot views the antibody molecule not necessarily as a major revenue driver but as an aide to the company’s oncology pipeline. |
By James Waldron Lantheus may have been hoping that “statistically significant” phase 3 data for its radioligand therapy would make a splash at ESMO, but not everyone is impressed. |
By Angus Liu In 2021, the FDA blasted Merck for using premature data to pursue a Keytruda approval in early-stage triple-negative breast cancer. Now, the PD-1 inhibitor has gold-standard overall survival data to back its case. |
By Angus Liu The same set of clinical data on Cabometyx and Tecentriq in prostate cancer has led to two distinct regulatory plans between Exelixis and its partner Ipsen. |
By Angus Liu Bayer is targeting a broader use of Nubeqa in metastatic hormone-sensitive prostate cancer with a combination free of chemotherapy. |
By Kevin Dunleavy One year after reporting a split result on Merck’s Welireg in a key phase 3 trial, the song remains the same for the kidney cancer drug as it continues to show benefits in progression-free survival but no significant improvement in overall survival when compared to Novartis’ chemotherapy Afinitor. Merck presented the results at the European Society of Medical Oncology Congress in Barcelona. |
By James Waldron Jazz Pharmaceuticals has posted fresh phase 2 data on zanidatamab that show the HER2-targeted bispecific antibody kept 59% of people with metastatic gastroesophageal cancer alive for at least 30 months. |
By Fraiser Kansteiner To bolster Enhertu's case in HER2-positive breast cancer, AstraZeneca and Daiichi Sankyo have rolled out positive data for the antibody-drug conjugate in patients who have brain metastases. |
By Conor Hale Presented at the annual meeting of the European Society for Medical Oncology, Exact Sciences said the latest findings may put its upcoming blood screener in the same realm as a fecal immunochemical test in the detection of advanced precancerous lesions. |
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