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Lisata Therapeutics (8NE) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Gemcitabine, Nab-paclitaxel, CertepetidePancreas Adenocarcinoma, Pancreatic Ductal Adenocarcinoma, Metastatic Pancreatic Cancer, Pancreas Cancer, Pancreatic Carcinoma, Unresectable Pancreatic Cancer, Pdac, Pdac - Pancreatic Ductal Adenocarcinomaphase1AndPhase2WithdrawnCertepetide Phase 1b/2a Continuous Infusion Trial in mPDACSep 09, 2024―
Gemcitabine, Durvalumab, Cisplatin, Certepetide, Folfox RegimenBile Duct Cancer, Cholangiocarcinoma, Intrahepatic Cholangiocarcinoma, Gall Bladder Cancer, Gall Bladder Carcinoma, Gallbladder Cancer, Gallbladder Carcinoma, Extrahepatic CholangiocarcinomaPhase IIActive Not RecruitingA Study of LSTA1 When Added to Standard of Care Versus Standard of Care Alone in Patients With Advanced Solid TumorsJan 26, 2023―

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 Lisata Therapeutics, Inc. (DE:8NE) have in its pipeline
Lisata Therapeutics DE:8NE is currently developing the following drugs: Gemcitabine, Nab-paclitaxel, Certepetide, Gemcitabine, Durvalumab, Cisplatin, Certepetide, Folfox Regimen. These drug candidates are in various stages of clinical development as the company works toward FDA approval.