Melanoma Clinical Trial

A Study Evaluating the Safety and Efficacy of ENV-101 (Taladegib) in Patients With Advanced Solid Tumors Harboring PTCH1 Loss of Function Mutations

Summary

This study employs a 2-stage design that aims to evaluate the efficacy and safety of ENV- 101, a potent Hedgehog (Hh) pathway inhibitor, in patients with refractory advanced solid tumors characterized by loss of function (LOF) mutations in the Patched-1 (PTCH1) gene. Stage 1 of this study will enroll approximately 44 patients randomized between two dose levels. As appropriate, Stage 2 of the study will expand enrollment based on the results of Stage 1.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Females or males greater than or equal to 18 years of age. Females and males between 12 and 17 years of age (inclusive) may be enrolled if deemed appropriate after review of an X-ray with the sponsor for evaluation of growth plate development
Has histologically or cytologically confirmed solid tumor that harbors a PTCH1 loss of function mutation, identified via genomic sequencing routinely performed at a CLIA certified laboratory
Able to take medication orally
Patients must be refractory to all standard of care therapy, or standard or curative therapy does not exist, or the patient has documented their refusal of standard of care therapies
Patients willing to sign and have a full understanding of the informed consent form
Life expectancy of ≥ 3 months

Exclusion Criteria:

Concurrent administration of any anti-cancer therapies (e.g., chemotherapy, other targeted therapy) other than those administered in this study
Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures. Patients with indwelling catheters are allowed
Malignancies other than the primary tumor type within 5 years prior to study start, with the exception of those with a negligible risk of metastasis or death (e.g., expected 5-year OS > 90%) treated with expected curative outcome (prior history of in situ basal or squamous cell skin cancer if completely excised, localized prostate cancer that is managed by surveillance, ductal carcinoma in situ treated surgically with curative intent are allowed)
History of clinically significant autoimmune disease requiring prescription systemic therapy in the last two years prior to study start; patients with controlled hypothyroidism may be considered after evaluation by the Investigator.
Presence of active infection at study start or confirmed active human immunodeficiency virus (HIV), Hepatitis B virus (HBV), or Hepatitis C virus (HCV)
Significant cardiovascular disease, such as New York Heart Association cardiac disease (Class II or greater), myocardial infarction within 3 months prior to study start, unstable arrhythmias, or unstable angina. Patients with known coronary artery disease, congestive heart failure not meeting the above criteria, or left ventricular ejection fraction < 50% must be on a stable medical regimen that is optimized in the opinion of the treating physician
Refractory nausea and vomiting, malabsorption, external biliary shunt or significant bowel resection that would preclude adequate absorption of investigational product
Major surgical procedure within 28 days prior to study start or anticipation of need for a major surgical procedure during the course of the study
Treatment with any other investigational agent or participation in another clinical study with therapeutic intent within 28 days prior to study start
Use of drugs that are known moderate or stronger CYP3A4 inhibitors or inducers within 12 days prior to study start
Unresolved toxicity of ≥ CTCAE Grade 2 attributed to any prior therapies (excluding anemia, alopecia, skin pigmentation, platinum-induced neurotoxicity and endocrine disease or ailments that are stable)
Males and females of reproductive potential who are sexually active and unwilling to use birth control for the duration of the study and for 30 days after their final study dose
Females that are pregnant or nursing
Females and males that are unwilling to refrain from blood or blood product donation for the duration of the study and for 30 days after their final study dose
Males who are unwilling to refrain from sperm donation for the duration of the study and for 30 days after their final study dose
Patients with a history of a severe allergic reaction, anaphylactic reaction or known hypersensitivity to any component of ENV-101
Patients who are immediate family members (spouse, parent, child, or sibling; biological or legally adopted) of personnel directly affiliated with a study investigative site or the study Sponsor

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

44

Study ID:

NCT05199584

Recruitment Status:

Recruiting

Sponsor:

Endeavor Biomedicines, Inc.

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There are 17 Locations for this study

See Locations Near You

Research Site
Los Angeles California, 90095, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
San Diego California, 92093, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Santa Monica California, 90404, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Tampa Florida, 33511, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Covington Louisiana, 70433, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Las Vegas Nevada, 89102, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
New York New York, 10065, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Durham North Carolina, 27710, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Cincinnati Ohio, 45229, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Cleveland Ohio, 44106, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Columbus Ohio, 43210, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Pittsburgh Pennsylvania, 15232, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Nashville Tennessee, 37203, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Houston Texas, 77030, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Fredericksburg Virginia, 22408, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Lynchburg Virginia, 24501, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]
Research Site
Madison Wisconsin, 53792, United States More Info
Endeavor Clinical Trials
Contact
858-727-3199
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Melanoma

Phase:

Phase 2

Estimated Enrollment:

44

Study ID:

NCT05199584

Recruitment Status:

Recruiting

Sponsor:


Endeavor Biomedicines, Inc.

How clear is this clinincal trial information?

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