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Recruiting Phase 1

A Phase 1 Study of XL309 (ISM3091) Alone and in Combination in Participants With Advanced Solid Tumors

NCT05932862 · tracked via the Priya Life Science USA tracker
Sponsor
Phase
Phase 1
Started
2024-04-03
Last updated
2025-09-05

Condition(s) studied

Advanced Solid Tumor

Investigational drug(s) / intervention(s)

XL309Olaparib →

XL309: XL309 will be administered orally per assigned schedule.

Olaparib: Olaparib will be administered orally per assigned schedule.

Study summary

This is a first-in-human (FIH), multicenter, open-label Phase I study to investigate the safety, tolerability, preliminary antitumor activity, as well as pharmacokinetics (PK) and pharmacodynamics of XL309 (previously ISM3091) administered alone or in combination with olaparib in participants with advanced solid tumors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria: 1. Capable of understanding and complying with protocol requirements. 2. Male or female aged 18 years or older. 3. Eastern Cooperative Oncology Group performance status 0 or 1. 4. Adequate bone marrow and organ function. 5. Participant-disease Characteristics Dose-Escalation Stage Single Agent and Combination: a) Participants whose tumor progressed on, or who were intolerant to standard therapy, have a disease for which no therapy exists or are not a candidate for these therapies, and have one of the following cancers: i. Histologically confirmed locally advanced/metastatic human epidermal growth factor receptor-2 (HER2)-negative breast cancer, with deleterious or suspected deleterious breast cancer gene (BRCA)1/2 alteration. ii. Histologically confirmed locally advanced/metastatic high-grade serous ovarian cancer (HGSOC), including primary peritoneal cancer (PPC) and fallopian tube cancer (FTC). iii. Histologically confirmed locally advanced/metastatic CRPC, with deleterious or suspected deleterious BRCA1/2 alteration. iv. Histologically confirmed locally advanced/metastatic pancreatic cancer with deleterious or suspected deleterious BRCA1/2 alteration. v. Locally advanced/metastatic tumors with deleterious or suspected deleterious germline or somatic homologous recombination repair (HRR) mutation or homologous recombination deficiency (HRD) phenotype. Cohort-Expansion Stage Single Agent and Combination: b) HER2-negative breast cancer cohort: participants with histologically confirmed locally advanced/metastatic (HER2)-negative breast cancer with alterations in select HRR genes. c) Platinum-sensitive HGSOC cohort: participants with histologically confirmed locally advanced/metastatic HGSOC, including primary peritoneal cancer (PPC) and fallopian tube cancer (FTC), with positive HRD result using an approved diagnostic, and/or alterations in select HRR genes. d) mCRPC cohort: participants with metastatic, castration-resistant adenocarcinoma of the prostate with alterations in select HRR genes. e) HRRm advanced solid tumors cohort: participants with locally advanced/metastatic tumors with alterations in select HRR genes. For all participants with solid tumors: 6. Participants in the Cohort-Expansion Stage must have at least 1 measurable target lesion. 7. Recovery to baseline or ≤ Grade 1 CTCAE v5 from AE(s) related to any prior treatments. Key Exclusion Criteria 1. Prior anticancer treatment including: 1. Small molecule-targeted therapy \< 5 half-lives from first dose of study treatment, or 3 weeks (whichever is shorter). 2. Any antibody therapy \< 5 half-lives from first dose of study treatment (or 4 weeks since last therapy, whichever is shorter). 3. Chemotherapy with nitrosoureas or mitomycin C \< 6 weeks from first dose of study treatment. Other chemotherapy \< 3 weeks prior to first dose of study treatment. 4. Radiation therapy (including radiofrequency ablation) \< 1 week prior to initiation of study treatment. Participants with clinically relevant ongoing complications from prior radiation therapy are not eligible. 2. Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks before first dose of study treatment. 3. History of hypersensitivity to any excipient of XL309, or history of allergic reactions attributed to drugs with a similar chemical or biologic structure or class to XL309. 4. Lactating or pregnant females. 5. Clinically relevant cardiovascular disease. 6. Known history of myelodysplastic syndrome. 7. Other severe, acute, or chronic medical condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or that may interfere with the interpretation of the study results, and in the judgment of the investigator, would make the participant inappropriate for the study. 8. Inability or unwillingness to comply with requirement for oral drug administration or presence of a gastrointestinal condition that would preclude adequate absorption of XL309. 9. Prior treatment with a ubiquitin specific peptidase 1 (USP1) inhibitor.

Primary outcome measure(s)

  • Dose Escalation Stage: Incidence of TEAEs and SAEs; AEs Leading to Dose Modification, Discontinuation, or Death; and Laboratory Abnormalities — Approximately 24 months
    Adverse events will be recorded and severity graded using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
  • Dose Escalation Stage: Incidence of Dose-Limiting Toxicities (DLTs) — Approximately 24 months
  • Dose Escalation Stage: XL309 Exposure Over Time Measured as Area Under the Plasma Concentration Curve (AUC) — Approximately 24 months
  • Dose Escalation Stage: XL309 Maximum Plasma Concentration (Cmax) — Approximately 24 months
  • Dose Escalation Stage: XL309 Time to Cmax — Approximately 24 months
  • Dose Escalation Stage: XL309 Trough Concentration (Ctrough) — Approximately 24 months
    Lowest concentration of drug in the bloodstream, measured just before the next dose is administered.
  • Dose Escalation Stage: XL309 Apparent Clearance (CL/F) — Approximately 24 months
  • Cohort Expansion Stage: Incidence of TEAEs and SAEs; AEs Leading to Dose Modification, Discontinuation, or Death; and Laboratory Abnormalities — Approximately 24 months
    Adverse events will be recorded and severity graded using CTCAE version 5.0.
  • Cohort Expansion Stage: Objective Response Rate (ORR) — Approximately 24 months
    ORR will be measured per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, as assessed by the Investigator. ORR for prostate cancer will be based on Prostate Cancer Working Group 3 (PCWG3) criteria, as assessed by the Investigator

Trial sites (16)

FacilityCityRegionStatus
Exelixis Clinical Site #12 Fountain Valley California Withdrawn
Exelixis Clinical Site #15 Jacksonville Florida Recruiting
Exelixis Clinical Site #8 Orlando Florida Recruiting
Exelixis Clinical Site #16 Tampa Florida Recruiting
Exelixis Clinical Site #14 Rochester Minnesota Recruiting
Exelixis Clinical Site #10 Kansas City Missouri Withdrawn
Exelixis Clinical Site #9 New Brunswick New Jersey Recruiting
Exelixis Clinical Site #5 New York New York Recruiting
Exelixis Clinical Site #7 Cleveland Ohio Recruiting
Exelixis Clinical Site #13 Oklahoma City Oklahoma Recruiting
Exelixis Clinical Site #11 Germantown Tennessee Recruiting
Exelixis Clinical Site #6 Nashville Tennessee Recruiting
Exelixis Clinical Site #4 Austin Texas Recruiting
Exelixis Clinical Site #1 Houston Texas Recruiting
Exelixis Clinical Site #2 Houston Texas Withdrawn
Exelixis Clinical Site #3 San Antonio Texas Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05932862 on ClinicalTrials.gov ↗ ← All trials in the USA