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โ† Trials
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Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors

RecruitingPhase 1, Phase 2Ages 18 Years - anyAllEnsem Therapeutics
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In plain words

What the trial is, and whether it could suit you

Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Key Inclusion Criteria: * Metastatic or locally advanced and unresectable solid tumor that has progressed on or after at least one available therapy. * Tumor harboring an activating PIK3CA mutation detected in either tumor tissue or ctDNA. * At least 1 measurable lesion or evaluable disease per RECIST v1.1. * An ECOG performance status score of 0 or 1. * Adequate organ function. Additional key inclusion criterion for Parts B and C: \- Confirmed metastatic or locally advanced HR+/HER2- breast cancer not amenable to surgical resection with curative intent and must have received at least 1 prior CDK4/6 inhibitor and at least 1 prior anti-estrogen therapy. Key Exclusion Criteria: * Has history (within โ‰ค2 years before screening) of a solid tumor or hematological malignancy that is histologically distinct from the cancers being studied. * Has symptomatic brain or spinal metastases or a known or suspected history of untreated or uncontrolled central nervous system (CNS) involvement. * Has an established diagnosis of diabetes mellitus type 1 or has uncontrolled diabetes mellitus type 2. * Has received treatment with any local or systemic anticancer therapy or investigational anticancer agent within 14 days prior to start of treatment. * Has toxicities from previous anticancer therapies that have not resolved to baseline levels with the exception of alopecia and peripheral neuropathy. * Has had radiotherapy outside the target tumor lesions within 14 days prior to start of treatment.
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What it tests

  • ETX-636 dose escalation
  • ETX-636 dose escalation in combination with fulvestrant
  • ETX-636 dose expansion in combination with fulvestrant
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Where

15 sites
Hoag Memorial Hospital Presbyterian
Newport Beach, United States
UCSF Helen Diller Family Comprehensive Cancer Center
San Francisco, United States
Yale University, Yale Cancer Center
New Haven, United States
Beth Israel Deaconess Medical Center
Boston, United States
Dana-Farber Cancer Institute
Boston, United States
Carolina BioOncology Institute
Huntersville, United States
The University of Texas MD Anderson Cancer Center
Houston, United States
START
San Antonio, United States

โ€ฆand 7 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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