RecruitingPhase 1

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

An Open-Label, Multicenter Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of XL309 (ISM3091) as Single-Agent and Combination Therapy in Patients 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

In plain language

This study tests XL309 alone or with olaparib in adults with advanced solid tumors. It is the first study of XL309 in people and checks its safety, how the body handles it, and whether it may fight cancer.

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.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Be age 18 or older and able to understand and follow study rules.
  • Be fully active or able to do light work despite some limits on hard physical activity.
  • Have bone marrow and organs that work well enough for the study.
  • For the dose-finding stage, standard treatment must have failed, caused side effects you could not tolerate, been unavailable, or not been suitable for you.
  • For the dose-finding stage, have cancer that has grown nearby or spread: certain breast, ovarian, prostate, or pancreatic cancers, or another solid tumor. Most groups require certain gene changes or problems with how cancer cells repair DNA.
  • For the expansion stage, have certain advanced breast, ovarian, prostate, or other solid tumors with selected DNA-repair gene changes or test results. The ovarian group must have cancer that responds to platinum-based chemotherapy.
  • For the expansion stage, have at least one tumor that can be measured.
  • Side effects from past treatment must have returned to your usual level or be mild.

Who can't join

  • Had cancer treatment too recently. Required waiting times depend on the treatment. Ongoing important problems from radiation also exclude you.
  • Have cancer in the brain or the space around its outer covering, unless treated with radiation or surgery and stable for at least 4 weeks.
  • Have an allergy to an ingredient in XL309 or have had allergic reactions to similar drugs.
  • Are pregnant or breastfeeding.
  • Have significant heart or blood vessel disease, or a history of myelodysplastic syndrome, a disorder in which bone marrow makes abnormal blood cells.
  • Have another serious health problem or abnormal lab result that the study doctor believes could make the study unsafe or affect its results.
  • Cannot or will not take medicine by mouth, or have a stomach or bowel condition that prevents your body from absorbing enough XL309.
  • Have previously taken a USP1 inhibitor, a drug that blocks a protein called USP1.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

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.

Study sites (16)

CA

FL

MN

MO

NJ

NY

OH

OK

TN

TX