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Home»Posts tagged with»oncology regulation

Merck strengthens its women’s oncology position with KEYNOTE-B96 overall survival results

By Pallavi Madhiraju on March 1, 2026   Pharma & Biotech  

Merck strengthens its women’s oncology position with KEYNOTE-B96 overall survival results

KEYNOTE-B96 shows overall survival gains for pembrolizumab in platinum-resistant ovarian cancer. Find out why this trial could reshape treatment strategy.

Real-world data meets legal limits as Bayer targets ERLEADA claims in prostate cancer

By Pallavi Madhiraju on February 28, 2026   Pharma & Biotech  

Real-world data meets legal limits as Bayer targets ERLEADA claims in prostate cancer

Bayer’s lawsuit against Johnson and Johnson raises critical questions about real-world evidence and oncology marketing. Read what this means for drug claims.

Why ImmunityBio’s ANKTIVA European launch could reshape BCG-unresponsive bladder cancer care

By Pallavi Madhiraju on February 20, 2026   Pharma & Biotech  

Why ImmunityBio’s ANKTIVA European launch could reshape BCG-unresponsive bladder cancer care

ImmunityBio expands ANKTIVA into Europe with Accord Healthcare. Discover what this means for bladder cancer care, regulation, and real-world adoption.

What Genentech’s Lunsumio VELO approval means for relapsed follicular lymphoma treatment

By Pallavi Madhiraju on December 22, 2025   Pharma & Biotech  

What Genentech’s Lunsumio VELO approval means for relapsed follicular lymphoma treatment

FDA approves subcutaneous Lunsumio VELO for relapsed follicular lymphoma. Explore what this changes for bispecific antibodies and outpatient cancer care.

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