A Study of IDP-001 in Advanced or Metastatic Solid Tumors
Sponsor: InduPro, Inc. • ClinicalTrials.gov ID: NCT07602842
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This clinical study is to evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of IDP-001 in participants with advanced or metastatic squamous and non-squamous NSCLC and other squamous cell solid tumors (for example, head and neck, esophageal, cervical, cutaneous).
Interventions
-
IDP-001
(Drug)
IV infusion
Eligibility criteria
Conditions
Locations
- START Los Angeles — Los Angeles, California, United States
- Florida Cancer Specialists — Sarasota, Florida, United States
- Community Cancer Center North — Indianapolis, Indiana, United States
- Roswell Park Cancer Institute — Buffalo, New York, United States
- START New York Long Island — Lake Success, New York, United States
- START Dallas Forth Worth — Fort Worth, Texas, United States
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Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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