Medicus Pharma Submits Protocol SKNJCT-005 To FDA Under Existing IND Application, For SkinJect Into Registrational Development For Patients With Gorlin Syndrome
Medicus Pharma Receives $22M In Non-Dilutive Financing
Medicus Pharma sees catalyst-rich year ahead as SkinJect and Teverelix progress
Medicus Pharma Reports First Quarter 2026 Financial Results and Provides Corporate Update
Medicus Pharma Q1 EPS $(0.31) Misses $(0.19) Estimate
EXCLUSIVE: Medicus Sees Strongest Efficacy At Higher Dose In Skin Cancer Study
Medicus Pharma reports strong Phase 2 dose response in skin cancer study
Medicus Pharma highlights positive dose-response in updated skin cancer trial results
Medicus Pharma Announces Results from Pre-Specified Expanded Phase 2 SKNJCT-003 Data Analysis Demonstrating Positive Dose-Response
Medicus Pharma Highlights Results From Pre-Specified Expanded Phase 2 SKNJCT-003 Data Analysis; Says Data Reveal 'a clear and consistent dose-response relationship across endpoints'
Medicus Pharma lobbies Congress on SkinJect regulatory pathway for rare Gorlin syndrome
Medicus Pharma CEO meets with lawmakers on Energy & Commerce Committee on Capitol Hill
Medicus Pharma advances Skinject in rare disease – ICYMI
Medicus Pharma files Orphan Drug application for SkinJect in rare skin Cancer indication
Medicus Pharma seeks orphan drug status for SkinJect in rare skin cancer disorder
Medicus Pharma Submits Orphan Drug Designation Application to U.S. FDA for SkinJect® in Gorlin Syndrome
Medicus Pharma Files Orphan Drug Designation To FDA For SkinJect To Treat Basal Cell Carcinoma In Participants With Gorlin Syndrome
Medicus Pharma to Present New Teverelix Data at AACE 2026 Demonstrating Long-Acting Hormone Suppression
Medicus Pharma to present new Teverelix data at upcoming endocrinology meeting
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