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Home»Posts tagged with»nab-paclitaxel

Phanes Therapeutics’ spevatamig data puts cold-tumor immunotherapy back in focus at ASCO 2026

By Pallavi Madhiraju on May 29, 2026   Pharma & Biotech  

Phanes Therapeutics’ spevatamig data puts cold-tumor immunotherapy back in focus at ASCO 2026

See how Phanes Therapeutics’ spevatamig data could reshape metastatic pancreatic cancer drug development after ASCO 2026.

ROSELLA trial at ASCO 2026: Corcept’s Lifyorli subgroup data and what it means for platinum-resistant ovarian cancer practice

By Pallavi Madhiraju on April 22, 2026   Pharma & Biotech  

ROSELLA trial at ASCO 2026: Corcept’s Lifyorli subgroup data and what it means for platinum-resistant ovarian cancer practice

Corcept presents Lifyorli ROSELLA phase 3 overall survival data by prior taxane use at ASCO 2026. What the subgroup analysis means for prescribers, payers, and the EMA review. Read now.

Why Corcept Therapeutics now faces a bigger execution test after Lifyorli’s ROSELLA success

By Pallavi Madhiraju on April 12, 2026   Pharma & Biotech  

Why Corcept Therapeutics now faces a bigger execution test after Lifyorli’s ROSELLA success

Corcept Therapeutics’ Lifyorli showed strong survival benefit in ovarian cancer. Read what the ROSELLA data could change for clinicians and payers.

Can Corcept’s Lifyorli become a real new standard in platinum-resistant ovarian cancer after FDA approval?

By Pallavi Madhiraju on March 26, 2026   Pharma & Biotech  

Can Corcept’s Lifyorli become a real new standard in platinum-resistant ovarian cancer after FDA approval?

Corcept’s Lifyorli won FDA approval in platinum-resistant ovarian cancer. Read what the survival data could change for clinicians, rivals, and regulators.

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.

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