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OncoMatch/Clinical Trials/NCT06533059

A Study to Learn About Study Medicine ALTA2618 in Adults With AKT1 E17K-Mutant Solid Tumors

Is NCT06533059 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies ALTA2618 for cancer.

Phase 1RecruitingAlterome Therapeutics, Inc.NCT06533059Data as of May 2026

Treatment: ALTA2618The purpose of this study is to characterize the safety and tolerability of ALTA2618 in adults with AKT1 E17K-mutant advanced solid tumors.

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Extracted eligibility criteria

Cancer type

Breast Carcinoma

Endometrial Cancer

Tumor Agnostic

Biomarker criteria

Required: AKT1 E17K

solid tumor malignancy harboring AKT1 E17K mutation identified through molecular testing (NGS- or PCR-based)

Excluded: KRAS genomic alteration

Patients known to have KRAS...genomic alterations in their tumor

Excluded: NRAS genomic alteration

Patients known to have NRAS...genomic alterations in their tumor

Excluded: HRAS genomic alteration

Patients known to have HRAS...genomic alterations in their tumor

Excluded: BRAF genomic alteration

Patients known to have BRAF...genomic alterations in their tumor

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: standard-of-care therapy

Progressed on, intolerant to, or declined prior standard-of-care therapy (including targeted therapy, if applicable) appropriate to tumor type and stage

Cannot have received: PI3K inhibitor

Prior treatment with PI3K and/or mTOR inhibitors

Cannot have received: mTOR inhibitor

Prior treatment with PI3K and/or mTOR inhibitors

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ function.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Research Site · La Jolla, California
  • Research Site · Los Angeles, California
  • Research Site · Denver, Colorado
  • Research Site · Sarasota, Florida
  • Research Site · Atlanta, Georgia

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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