Home » Posts tagged with» Inc. (Page 2)
By Soujanya Ravi on April 7, 2026
Pharma & Biotech
Can SIM0505’s Fast Track win accelerate NextCure’s ovarian cancer strategy? Read the full PDN analysis on risks, ASCO data, and regulatory outlook.
By Pallavi Madhiraju on April 7, 2026
Pharma & Biotech
Vyome’s VT-1953 heads to AACR 2026 with Phase 2 data in malignant fungating wounds. Read what this could change for supportive oncology.
By Soujanya Ravi on April 1, 2026
Pharma & Biotech
Calidi Biotherapeutics, Inc. unveils new RedTail and TROP-2 data at AACR 2026. Read what this means for solid tumor immunotherapy and CLD-401 next.
By Soujanya Ravi on April 1, 2026
Medical Devices & Diagnostics
electroCore, Inc.’s latest data could reshape bioelectronic medicine in trauma-related brain injury. Read what clinicians and industry watchers may track next.
By Soujanya Ravi on April 1, 2026
Pharma & Biotech
Discover what Ocugen, Inc.’s OCU410ST milestone means for the future of inherited retinal blindness treatment and the race toward first approval.
By Soujanya Ravi on April 1, 2026
Pharma & Biotech
Cogent Biosciences files bezuclastinib NDA in second-line GIST. Explore what the PEAK data could change for clinicians, regulators, and investors.
By Pallavi Madhiraju on March 31, 2026
Pharma & Biotech
Merck’s enlicitide decanoate beat oral rivals in Phase 3. Read what this could change for cholesterol care, PCSK9 adoption, and market strategy.
By Pallavi Madhiraju on March 30, 2026
Pharma & Biotech
Can Merck turn WINREVAIR’s CADENCE data into a new treatment path in CpcPH-HFpEF? Read the full analysis of what changes next.
By Soujanya Ravi on March 29, 2026
Pharma & Biotech
CADENCE trial data shows sotatercept’s promise in HFpEF-linked pulmonary hypertension. Find out what this means for treatment and regulation.
By Pallavi Madhiraju on March 27, 2026
Pharma & Biotech
NEOK002 has cleared the FDA IND stage. Read why this bispecific ADC matters for solid tumors, clinical strategy, and the next phase of ADC competition.