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Castle Biosciences Presents Data at the Dermatology Nurses’ Association 2021 Annual Convention

BioTech 365

Castle Biosciences Presents Data at the Dermatology Nurses’ Association 2021 Annual Convention Castle Biosciences Presents Data at the Dermatology Nurses’ Association 2021 Annual Convention FRIENDSWOOD, Texas–(BUSINESS WIRE)–$CSTL #DNANurses–Castle Biosciences, Inc.

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Clinical Catch-Up: January 18-22 | BioSpace

The Pharma Data

National Institute of Allergy and Infectious Diseases (NIAID), of bamlanivimab (LY-CoV555) decreased the risk of COVID-19 among residents and staff of long-term care facilities, i.e., nursing homes. Quantum Genomics launched its Phase III REFRESH trial in difficult-to-treat or resistant hypertension.

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CheckMate -577, a Phase 3 Trial Evaluating Opdivo (nivolumab) as Adjuvant Therapy for Patients with Resected Esophageal or Gastroesophageal Junction Cancer, Meets Primary Endpoint of Disease-Free Survival

The Pharma Data

1%) as determined by an FDA-approved test, with no EGFR or ALK genomic tumor aberrations. Patients with EGFR or ALK genomic tumor aberrations should have disease progression on FDA-approved therapy for these aberrations prior to receiving OPDIVO. Immune-Mediated Skin and Dermatologic Adverse Reactions. Serious Adverse Reactions.

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CheckMate -649, a Phase 3 Trial Evaluating Opdivo (nivolumab) Plus Chemotherapy vs. Chemotherapy, Meets Primary Endpoints Demonstrating Superior Overall Survival and Progression-Free Survival in First-Line Treatment of Gastric and Esophageal Cancers

The Pharma Data

1%) as determined by an FDA-approved test, with no EGFR or ALK genomic tumor aberrations. Patients with EGFR or ALK genomic tumor aberrations should have disease progression on FDA-approved therapy for these aberrations prior to receiving OPDIVO. Immune-Mediated Skin and Dermatologic Adverse Reactions. Serious Adverse Reactions.

Trials 52