Skip to main content
OpenTrials
Completed

NCT Number: NCT03888612

Trial of ARV-110 in Patients With Metastatic Castration Resistant Prostate Cancer

Phase 1/2 dose escalation study to assess the safety and tolerability of ARV-110 in men with mCRPC who have progressed on prior approved systemic therapies for their castrate resistant disease (one of which must be enzalutamide or abiraterone).

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Prostate Cancer Metastatic Genital Diseases Genital Diseases, Male Genital Neoplasms, Male Male Urogenital Diseases Neoplasms Neoplasms by Site Prostatic Diseases Prostatic Neoplasms Urogenital Diseases Urogenital Neoplasms

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Clinical Trial Site, Los Angeles, California, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Part A:

  • Patients must be male and at least 18 years of age at the time of signing the informed consent.
  • Patients must present with histological, pathological, or cytological confirmed diagnosis of advanced or metastatic castration resistant adenocarcinoma of the prostate.
  • Patients must have progressed on at least 2 prior approved systemic therapies for CRPC (at least one must be abiraterone or enzalutamide).
  • Patients with progressive mCRPC
  • Patients must have ongoing ADT with a gonadotropin releasing hormone analog or inhibitor, or orchiectomy (surgical or medical castration).

Part B:

  • Patients must be male and at least 18 years of age at the time of signing the informed consent.
  • Patients must present with histological, pathological, or cytological confirmed diagnosis of advanced or metastatic castration resistant adenocarcinoma of the prostate.
  • Patients must have received at least one but no more than two prior second generation anti-androgen agents (e.g., enzalutamide or abiraterone) for CRPC.
  • Patients must have received no more than one prior chemotherapy regimen in each of the following settings: castrate sensitive and castrate resistant prostate cancer.
  • Patients must have ongoing ADT with a gonadotropin releasing hormone analog or inhibitor, or orchiectomy (surgical or medical castration).

Part B - Phase 2 Expansion Cohort Subgroup 4

  • Patient has received only one prior AR second generation therapy (e.g., abiraterone or enzalutamide) either as treatment for CSPC or CRPC and no more than 1 regimen in CRPC setting.
  • No prior chemotherapy

Exclusion criteria

Part A:

  • Patients with known symptomatic brain metastases requiring steroids (above physiologic replacement doses)
  • Major surgery (as defined by the Investigator) within 4 weeks of first dose of study drug.
  • Radiation therapy within 4 weeks of first dose of study drug or prior irradiation to >25% of the bone marrow. Palliative radiation for the alleviation of pain due to bone metastasis will be allowed during the study
  • Systemic anti cancer therapy within 2 weeks of first dose of study drug (6 weeks for bicalutamide, mitomycin C, or nitrosoureas and 4 weeks for abiraterone). Patients are ineligible if they received any other type of anti cancer agent (except agents to maintain castrate status) within 2 weeks before first dose of study drug.

Part B:

  • Patients with known symptomatic brain metastases requiring steroids (above physiologic replacement doses)
  • Major surgery (as defined by the Investigator) within 4 weeks of first dose of study drug.
  • Radiation therapy within 4 weeks of first dose of study drug or prior irradiation to >25% of the bone marrow. Palliative radiation for the alleviation of pain due to bone metastasis will be allowed during the study
  • Systemic anti cancer therapy within 2 weeks of first dose of study drug (6 weeks for bicalutamide, mitomycin C, or nitrosoureas and 4 weeks for abiraterone). Patients are ineligible if they received any other type of anti cancer agent (except agents to maintain castrate status) within 2 weeks before first dose of study drug.

Treatment and study plan

ARV-110

Drug

Part A: Daily oral dosages are predetermined by cohort review committee after the initial starting dose cohort after the first 28 days of treatment

Part B: Daily oral dosage and schedule at a recommended Phase 2 dose based on data from Part A

Primary outcomes

  1. Part A: Incidence of Dose Limiting Toxicities of ARV-110

    Time frame: 28 Days

    First Cycle Dose limiting toxicities characterized by type, frequency, severity (as graded by NCI CTCAE version 5.0), timing, seriousness, and relationship to study drug

  2. Part A: Number of Patients with Adverse Events as a measure of safety and tolerability of ARV-110

    Time frame: 28 Days

    Adverse events as characterized by type, frequency, severity (as graded by NCI CTCAE version 5.0), timing, seriousness, and relationship to study drug.

  3. Part A: Incidence of laboratory abnormalities as a measure of safety and tolerability of ARV-110

    Time frame: 28 Days

    Laboratory abnormalities as characterized by type, frequency, severity (as graded by NCI CTCAE version 5.0), and timing.

  4. Part B: Measurement of PSA response rate per PCWG3 accessing anti-tumor activity of ARV-110

    Time frame: 12 Weeks

    PSA response rate per PCWG3.

  5. Part B: Measurement of overall RECIST response rate accessing the anti-tumor activity of ARV-110

    Time frame: 12 Weeks

    Overall RECIST response rate in patients with measurable disease at baseline.

  6. Part B: To evaluate the clinical anti-tumor activity of ARV-110 in patients with mCRPC

    Time frame: 12 Weeks

    To evaluate the clinical anti-tumor activity (PSA response rate per PCWG3, Overall RECIST RR, rPFS, and PFS) of ARV-110 in patients with mCRPC in different subgroups of patients with mCRPC with predefined tumor genomic and molecular profiles or based on prior therapy.

Secondary outcomes

  1. Part A: Anti-tumor activity based on the overall PSA response in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the overall PSA response per PCWG3.

  2. Part A: Anti-tumor activity based on the overall RECIST response in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the overall RECIST response rate.

  3. Part A: Anti-tumor activity based on the progression free survival in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the time to event progression free survival.

  4. Part A: Anti-tumor activity based on the duration of response in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the duration of response.

  5. Part A: Anti-tumor activity based on the time to progression in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the time to progression.

  6. Part A: Anti-tumor activity based on the overall survival in the entire study population and in the subsets of patient based on the AR mutational status of their tumor.

    Time frame: 12 Weeks

    The anti-tumor activity of ARV-110 will be assessed by evaluating the overall survival.

  7. Part A: Concentration-time curve (AUC) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter area under the concentration-time curve (AUC).

  8. Part A: Maximum concentration (Cmax) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter maximum concentration (Cmax).

  9. Part A: Minimum concentration (Cmin) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter minimum concentration (Cmin).

  10. Part A: Time to maximum concentration (Tmax) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter time to maximum concentration (Tmax)

  11. Part B: Concentration-time curve (AUC) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter area under the concentration-time curve (AUC).

  12. Part B: Maximum concentration (Cmax) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter maximum concentration (Cmax).

  13. Part B: Minimum concentration (Cmin) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter minimum concentration (Cmin).

  14. Part B: Time to maximum concentration (Tmax) for single and multiple dose of ARV-110

    Time frame: 28 Days

    PK parameters will be assessed when applicable after a single dose and after multiple once and twice daily doses. Assessment of pharmacokinetic parameter time to maximum concentration (Tmax)

  15. Part B: Duration of response

    Time frame: 12 Weeks

    From the date of first confirmed best overall response of CR or PR to the date of first progression per RECIST 1.1 or PCWG3, or death due to any cause without evidence of radiographic progression, whichever occurs first.

  16. Part B: Overall survival

    Time frame: 12 Weeks

    Time interval from the date of first ARV-110 dose to the date of death due to any cause.

Sponsors and collaborators

Lead sponsor

Arvinas Inc.

Industry

Registry information

Official study title

A Phase 1/2, Open-label, Dose Escalation, and Cohort Expansion Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ARV-110 in Patients With Metastatic Castration Resistant Prostate Cancer

Acronym: mCRPC

Important dates

Study start
2019
Primary completion
2024
Study completion
2025
First posted
Mar 25, 2019
Registry last updated
Apr 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.