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TriSalus Life Sciences (TLSI)
NASDAQ:TLSI
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TriSalus Life Sciences (TLSI) Drug Pipeline

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Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Anti-Pd-1, Sd-101
Locally Advanced Pancreatic Adenocarcinoma
Phase I
Active Not Recruiting
Pressure Enabled Intrapancreatic Delivery of SD-101 With Checkpoint Blockade for Locally Advanced Pancreatic Adenocarcinoma
Oct 19, 2022
Pembrolizumab, Nivolumab, Ipilimumab, Sd-101
Hepatocellular Carcinoma, Intrahepatic Cholangiocarcinoma
Phase I/II
Terminated
Pressure Enabled Delivery of SD-101 With Checkpoint Blockade for Primary Liver Tumors
Jan 21, 2022
Nivolumab, Ipilimumab, Sd-101, Nivolumab And Relatlimab
Metastatic Uveal Melanoma In The Liver
Phase I
Terminated
Intrahepatic Delivery of SD-101 by Pressure-Enabled Regional Immuno-oncology (PERIO), With Checkpoint Blockade in Adults With Metastatic Uveal Melanoma
Jun 02, 2021

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 TriSalus Life Sciences (TLSI) have in its pipeline
      TLSI is currently developing the following drugs: Anti-Pd-1, Sd-101, Pembrolizumab, Nivolumab, Ipilimumab, Sd-101, Nivolumab, Ipilimumab, Sd-101, Nivolumab And Relatlimab. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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