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Lytix Biopharma AS (6BG) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Ltx-315 In Combination With PembrolizumabAdvanced MelanomaPhase IIUnknownIntratumoral Injection of LTX-315 in Combination With Pembrolizumab in Advanced MelanomaMar 02, 2021―
Ltx-315 And TilsSoft Tissue SarcomaPhase IICompletedLTX-315 and Adoptive T-cell Therapy in Advanced Soft Tissue Sarcoma (ATLAS-IT-04)Oct 02, 2018―
Ltx-315 Consecutive Lesions, Ltx-315, Ltx-315 + Ipilimumab, Ltx-315 + PembrolizumabCancer, Breast Cancer, Melanoma, Lymphoma, Head And Neck Cancer, Triple-Negative Breast CancerPhase ICompletedLTX-315 in Patients With Transdermally Accessible Tumours as Monotherapy or Combination With Ipilimumab or PembrolizumabOct 28, 2013―

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 Lytix Biopharma AS (DE:6BG) have in its pipeline
Lytix Biopharma AS DE:6BG is currently developing the following drugs: Ltx-315 In Combination With Pembrolizumab, Ltx-315 And Tils, Ltx-315 Consecutive Lesions, Ltx-315, Ltx-315 + Ipilimumab, Ltx-315 + Pembrolizumab. These drug candidates are in various stages of clinical development as the company works toward FDA approval.