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Carisma Therapeutics (CARM) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Ct-0525Her2-PositivePhase IActive Not RecruitingCAR-monocytes for the Treatment of HER2 Overexpressing Solid TumorsFeb 02, 2024―
Pembrolizumab, Ct-0508Prostate Cancer, Bladder Cancer, Ovarian Neoplasms, Colorectal Cancer, Breast Cancer, Cancer, Pancreatic Cancer, Endometrial Cancer, Head And Neck Cancer, Her2-Positive Breast Cancer, Her2-Positive Gastric Cancer, Biliary Tract Cancer, Carcinoma, Squamous, Adenocarcinoma, Lung Cancer, Small Cell, Carcinoma, Hepatocellular, Stomach Neoplasms, Carcinoma, Transitional Cell, Breast Neoplasm, Carcinoma, Small Cell, Esophagogastric Junction Neoplasms, Her-2 Protein Overexpression, Her2-Positive, Bile Duct Cancer, Carcinoma, Ductal, Lung Cancer, Non-Small-Cell, Carcinoma, Ovarian Epithelial, Inflammatory Breast Cancer, Malignant Neoplasms, Her2-Positive Solid Tumors, Her-2 Gene AmplificationPhase IActive Not RecruitingCAR-macrophages for the Treatment of HER2 Overexpressing Solid TumorsNov 23, 2020―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Carisma Therapeutics, Inc. (CARM) have in its pipeline
Carisma Therapeutics CARM is currently developing the following drugs: Ct-0525, Pembrolizumab, Ct-0508. These drug candidates are in various stages of clinical development as the company works toward FDA approval.