Open Actively Recruiting

Adenosine Receptor Antagonist Combination Therapy for Metastatic Castrate Resistant Prostate Cancer

About

Brief Summary

This is a Phase 1b/2, open-label, multicenter platform trial to evaluate the antitumor activity and safety of etrumadenant (AB928)-based combination therapy in participants with metastatic castrate resistant prostate cancer (mCRPC).

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase I/II

Eligibility

Gender
Male
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
N/A

General Inclusion Criteria:

  • Male participants; age ≥ 18 years
  • Metastatic castrate-resistant prostate cancer while on anti-androgen treatment with castrate levels of testosterone (≤1.7 nmol/L or 50 ng/dL)
  • Measurable or non-measurable disease as per radiographic evaluation
  • Participants with measurable disease may require a fresh tumor biopsy at study entry
  • Performance status of 0 or 1
  • Life expectancy of at least 3 months
  • Adequate hematologic and end-organ function
  • Inclusion Criteria for Participants receiving an enzalutamide-containing treatment
    • Disease progression after prior treatment with abiraterone
  • Inclusion Criteria for Participants receiving a docetaxel-containing treatment
    • Disease progression after prior androgen synthesis inhibitor therapy
  • Inclusion Criteria for all other Participants
    • Disease progression after prior androgen synthesis inhibitor treatment and up to 2 prior lines of taxane chemotherapy

General Exclusion Criteria:

  • Prior treatment with immune checkpoint blockade therapy
  • Prior anticancer treatment including approved agents, systemic radiotherapy, or investigational therapy, within 2-4 weeks prior first study treatment
  • ECG (Electrocardiogram) result with QTcF ≥480 msec
  • Prior stem cell or solid organ transplantation
  • Prior treatment with drugs that stimulate the immune system within 4 weeks prior to first study treatment
  • Prior treatment with drugs that suppress the immune system within 2 weeks prior to first study treatment
  • Received a live, attenuated vaccine within 4 weeks prior to first study treatment, or may need to receive a vaccine during study treatment
  • Presence of metastases in the brain or cancer spreading into the cerebrospinal fluid - CSF (leptomeningeal disease)
  • Prior pulmonary fibrosis, pneumonia, or pneumonitis
  • Cancer other than prostate within 2 years prior to study entry, except for some cancers with a low risk of spreading like non-melanoma skin
  • Prior treatment with an agent targeting the adenosine pathway
  • No oral or IV antibiotics within 2 weeks prior to first study treatment
  • No severe infection within 4 weeks prior to first study treatment
  • No clinically significant cardiac disease
  • Inability to swallow oral medications
  • HIV, Hepatitis B, and C test results negative prior to first study treatment
  • Exclusion Criteria for Participants receiving an enzalutamide-containing treatment
    • Prior treatment with docetaxel, cabazitaxel, or other taxane chemotherapy (prior docetaxel [up to 6 cycles] for hormone-sensitive prostate cancer is allowed if the last dose was at least 6 months prior to study treatment initiation)
    • Prior treatment with enzalutamide or similar therapy other than abiraterone
    • Active or history of autoimmune disease or immune deficiency
    • History of severe allergic reactions to antibody therapy
    • Concomitant use of a medication prohibited by the protocol (including certain transporter substrates as well as known strong CYP3A4 inducers and CYP3A4 inhibitors) within 4 weeks prior to and throughout study treatment
  • Exclusion Criteria for Participants receiving a docetaxel-containing treatment
    • Prior treatment with docetaxel, cabazitaxel, or other taxane chemotherapy
    • Active or history of autoimmune disease or immune deficiency
    • History of severe allergic reactions to antibody therapy
    • Concomitant use of a medication prohibited by the protocol (including certain transporter substrates as well as known strong CYP3A4 inducers and CYP3A4 inhibitors) within 4 weeks prior to and throughout study treatment
  • Exclusion Criteria for all other Participants
    • Prior treatment with 3 or more lines of taxane chemotherapy
    • Active or history of autoimmune disease or immune deficiency
    • History of severe allergic reactions to antibody therapy
    • Concomitant use of a medication prohibited by the protocol (including certain transporter substrates as well as known strong CYP3A4 inducers and CYP3A4 inhibitors) within 4 weeks prior to and throughout study treatment

Join this Trial

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Study Stats
Protocol No.
20-001001
Category
Hematology-Oncology
Oncology
Contact
KATHRYN B HILBURN
Location
  • UCLA Santa Monica
  • UCLA Westwood
For Providers
NCT No.
NCT04381832
For detailed technical eligibility, visit ClinicalTrials.gov.