Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors
A Phase 1/2, Open-label, First-in-human Study of the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ETX-636, a Pan-mutant-selective PI3Kα Inhibitor, as Monotherapy and in Combination With Other Anticancer Therapies in Participants With Advanced Solid Tumors
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
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 ≤2 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.
Study sites (10)
CA
- Hoag Memorial Hospital Presbyterian · Newport Beach, CA 92663Angela J Fuller · Study contact · 949-764-4891 · aj.fuller@hoag.orgMonica Mita, MD · Principal investigatorMore trials in Newport Beach
- UCSF Helen Diller Family Comprehensive Cancer Center · San Francisco, CA 94158Phu Lam · Study contact · 415-818-7994 · Phu.Lam@ucsf.eduVarun Monga, MD · Principal investigatorMore trials in San Francisco
CT
- Yale University, Yale Cancer Center · New Haven, CT 06520Carl Brown · Study contact · 203-785-4095 · carl.brown@yale.eduAdriana Kahn, MD · Principal investigatorMore trials in New Haven
MA
- Beth Israel Deaconess Medical Center · Boston, MA 02215Susan Gotthardt · Study contact · 617-975-7452 · sgotthar@bidmc.harvard.eduGerburg Wulf, MD · Principal investigatorMore trials in Boston
- Dana-Farber Cancer Institute · Boston, MA 02215CT.GOV Contact · Study contact · 877-338-7425Sarah Simmons, MD · Principal investigatorMore trials in Boston
NC
- Carolina BioOncology Institute · Huntersville, NC 28078Hannah Wall · Study contact · 980-441-1148 · hwall@carolinabiooncology.orgNeel Gandhi, MD · Principal investigatorMore trials in Huntersville
TX
- The University of Texas MD Anderson Cancer Center · Houston, TX 77030Jordi Rodon Ahnert, MD, PhD · Study contact · 713-792-5603Jordi Rodon Ahnert, MD, PhD · Principal investigatorMore trials in Houston
- START · San Antonio, TX 78229Isabel Jimenenz, RN, MSN · Study contact · 210-593-5265 · isabel.jimenez@startresearch.comAmita Patnaik, MD, FRPC · Principal investigatorMore trials in San Antonio
VA
- NEXT · Fairfax, VA 22031Maybelle De La Rosa · Study contact · 703-783-4518 · mdelarosa@nextoncology.comAlex Spira, MD, PhD, FACP · Principal investigatorMore trials in Fairfax
WA
- Fred Hutchinson Cancer Center · Seattle, WA 98109Kaysey Hermens · Study contact · 206-667-5715 · khermens@fredhutch.orgJennifer M Specht, MD · Principal investigatorMore trials in Seattle