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Merck wins first FDA approval for Keytruda as a treatment for mesothelioma
Merck & Co. Inc. said Wednesday the U.S. Food and Drug Administration has approved its blockbuster cancer drug Keytruda as a treatment for malignant plural mesothelioma, a rare cancer associated with asbestos.
USFDA nod to Merck KEYTRUDA plus Pemetrexed, Platinum Chemotherapy for Unresectable Advanced or Metastatic Malignant Pleural Mesothelioma
Rahway: Merck, known as MSD outside of the United States and Canada, has announced the U.S.Food and Drug Administration (FDA) has approved KEYTRUDA, Merck’s anti-PD-1 therapy, in combination
Keytruda Plus Chemotherapy Approved for Malignant Pleural Mesothelioma
The FDA has approved Keytruda in combination with pemetrexed and platinum chemotherapy, as first-line Tx of unresectable advanced or metastatic malignant pleural mesothelioma.
Pembrolizumab Approved With Chemotherapy for Malignant Pleural Mesothelioma
Pembrolizumab (Keytruda, Merck) has picked up another indication — this time for the first-line treatment of unresectable advanced or metastatic malignant pleural mesothelioma (MPM) in combination with pemetrexed and platinum chemotherapy.
FDA Approves Frontline Pembrolizumab/Chemotherapy in Advanced Mesothelioma
Pembrolizumab plus chemotherapy is now an approved frontline treatment for patients with unresectable advanced or metastatic malignant pleural mesothelioma.
Merck: KEYTRUDA Plus Chemotherapy Gets FDA Approval For Malignant Pleural Mesothelioma In Adults
Drug major Merck & Co., Inc. (MRK) announced Wednesday that the U.S. Food and Drug Administration has approved its anti-PD-1 therapy
Merck's Keytruda Obtains its First FDA Approval for Mesothelioma
Merck & Co., Inc. MRK announced that the FDA had approved its blockbuster anti-PD-1 therapy, Keytruda (pembrolizumab), for a new indication. The regulatory body has now approved Keytruda in combination with pemetrexed and platinum chemotherapy for the first-line treatment of adult patients with unresectable advanced or metastatic malignant pleural mesothelioma (MPM).
Merck’s Keytruda label expanded in the U.S. for mesothelioma
Merck (NYSE:MRK) announced Wednesday that the U.S. Food and Drug Administration (FDA) approved a label expansion for its blockbuster therapy Keytruda to allow its use as a first-line combination therapy for mesothelioma,
The Brighterside of News on MSN
4d
Breakthrough cancer treatment destroys advanced-stage tumors in under 6 days
Researchers from Rice University and Baylor College of Medicine have demonstrated a groundbreaking treatment that eradicates ...
Times Star
3h
Inquest: Michael Lee of Cleator died due to mesothelioma
AN inquest has been opened into the death of a Cleator man who suffered from a form of lung cancer associated with exposure to asbestos. Michael Lee, 74, died at his home on Hilden Road on July 1, ...
5d
$39M Jury Verdict Awarded in Novel Mesothelioma Case
Plaintiffs' lead attorney Mark Linder emphasized this is the first mesothelioma lawsuit that proceeded from this type of ...
23h
Best Mesothelioma Lawyers San Antonio, TX Of 2024
Mesothelioma is among the most dangerous illnesses that result from asbestos exposure. It involves tumors, typically ...
FiercePharma
7d
J&J talc appeal upends $260M award to Oregon woman with mesothelioma
Three months after a jury awarded $260 million to an Oregon woman who claimed her use of Johnson’s Baby Powder caused her to ...
devdiscourse
7d
Judge Overturns $260 Million Verdict Against Johnson & Johnson in Talc Mesothelioma Case
A state judge in Oregon has overturned a $260 million verdict against Johnson & Johnson in a mesothelioma lawsuit. The judge ...
Acsh.org
4d
On the Toxic Tort Docket
Recent surprise decisions have upended plaintiffs’ expectations on the toxic tort front. In Delaware, the top court is ...
3d
Son of Cannock mine worker appealing for help after seeing father's 'unjust' and 'painful' death
The son of a former mining surveyor has spoken of the anguish of discovering his father's asbestos-related cancer diagnosis, ...
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Keytruda
Pembrolizumab
Merck & Co.
Food and Drug Administration
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