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Home»Posts tagged with»FDA guidance

Theriva Biologics leverages FDA and EMA feedback to optimize VCN-01 pivotal trial

By Soujanya Ravi on March 24, 2026   Pharma & Biotech  

Theriva Biologics leverages FDA and EMA feedback to optimize VCN-01 pivotal trial

Theriva Biologics advances VCN-01 into phase 3 for metastatic pancreatic cancer with FDA and EMA guidance. Explore trial design, dosing strategy, and risks.

Frontage expands US–China clinical footprint to meet demand for early phase integration

By Pallavi Madhiraju on February 2, 2026   Pharma & Biotech  

Frontage expands US–China clinical footprint to meet demand for early phase integration

Frontage Laboratories expands US and China early phase clinical sites with radiolabel, BE, and oncology focus. Find out what this means for CRDMOs in 2026.

Why Aviva Bio’s deuterated testosterone may change hormone therapy for women

By Pallavi Madhiraju on January 26, 2026   Pharma & Biotech  

Why Aviva Bio’s deuterated testosterone may change hormone therapy for women

Aviva Bio’s AVA‑291 receives FDA development feedback for women’s testosterone therapy. See what makes it safer and what happens next in clinical trials.

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