Merck has announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA® (pembrolizumab), as well as the newly approved subcutaneous formulation KEYTRUDA QLEx™, in combination with WELIREG® (belzutifan) for the adjuvant treatment of certain patients with renal cell carcinoma (RCC), the most common form of kidney cancer.

As healthcare delivery becomes increasingly team-oriented, pharmaceutical marketers are being encouraged to look beyond physicians and engage a broader network of healthcare professionals involved in patient care. According to a recent announcement from IQVIA Digital, artificial intelligence is helping marketers identify and connect with nurse practitioners (NPs), physician associates (PAs), and other key members of collaborative care teams who play a growing role in treatment decisions.

National Forensic Sciences University is an Institution of National Importance under Ministry of Home Affairs, Government of India. It is the one and only university in the world dedicated to the Forensic Sciences. The institution is established by the act of Parliament in October 2020.

Eli Lilly has announced positive Phase 3 results showing that its BTK inhibitor Jaypirca (pirtobrutinib) significantly improved outcomes for patients with previously treated chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) when combined with a fixed-duration venetoclax-based regimen. The findings add to growing evidence that targeted combination therapies may help patients achieve longer periods of disease control without continuous treatment.

Lundbeck has unveiled promising early-stage clinical data for its investigational therapy asedebart, highlighting a potential new treatment approach for patients living with Cushing’s disease, a rare endocrine disorder driven by excessive cortisol production. The findings were presented at the ENDO 2026 Annual Meeting in Chicago.

Johnson & Johnson has reported encouraging Phase 3 results for a combination therapy featuring TALVEY (talquetamab-tgvs) and DARZALEX FASPRO (daratumumab and hyaluronidase-fihj), highlighting the growing potential of bispecific antibody-based treatment strategies in earlier-line relapsed or refractory multiple myeloma (RRMM).