Study to Assess Abivertinib in Combination With Abiraterone in Metastatic Castration Resistant Prostate Cancer
Study Details
Study Description
Brief Summary
This is a phase 2, multicenter, open-label study to evaluate the efficacy of abivertinib with abiraterone in patients with metastatic castration-resistant prostate cancer.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
This is a phase 2, multicenter, open-label study to evaluate the efficacy of abivertinib with abiraterone in patients with metastatic castration-resistant prostate cancer via assessment of 6-month radiographic progression-free survival. The study will include two cohorts, abiraterone-naive and abiraterone-progressing.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Abivertinib - Abiraterone-naive Abiraterone-naive: Abivertinib 200 mg by mouth twice daily with abiraterone 1000 mg by mouth daily. |
Drug: Abivertinib
Abivertinib is a small molecule inhibitor
Other Names:
Drug: Abiraterone
Hormone-based chemotherapy
|
| Experimental: Abivertinib - Abiraterone-progressing Abiraterone-progressing: Abivertinib 200 mg by mouth twice daily with abiraterone 1000 mg by mouth daily. |
Drug: Abivertinib
Abivertinib is a small molecule inhibitor
Other Names:
Drug: Abiraterone
Hormone-based chemotherapy
|
Outcome Measures
Primary Outcome Measures
- 6-month radiographic progression-free survival [baseline through study completion at up to approximately 63 months]
6-month radiographic progression-free survival (rPFS) will be assessed as defined by percent of subjects alive and without progression by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 for measurable disease and Prostate Cancer Working Group 3 (PCWG3) criteria for bone metastases.
Secondary Outcome Measures
- Overall Response Rate [baseline through study completion at up to approximately 63 months]
Overall Response Rate (ORR) will be defined by percent of subjects alive and without progression by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
- Duration of response [baseline through study completion at up to approximately 63 months]
duration of response will be defined as the time from the first documented response in patients with measurable disease to the date of progression or death due to any cause.
- Prostate-Specific Antigen (PSA) progression [baseline through study completion at up to approximately 63 months]
Change in PSA as compared to baseline as defined by Prostate Cancer Working Group 3 (PCWG3) criteria
- Safety and tolerability [baseline through study completion at up to approximately 63 months]
Safety and tolerability of abivertinib with abiraterone using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 criteria.
- Time to occurrence of first skeletal event [baseline through study completion at up to approximately 63 months]
Time to occurrence of first symptomatic skeletal event will be defined as the time from enrollment to the first symptomatic skeletal event defined as use of external beam radiotherapy to relieve skeletal symptoms or the occurrence of new symptomatic pathological bone fractures (vertebral or non-vertebral) or the occurrence of spinal cord compression or a tumor related orthopedic surgical intervention.
- Time to first subsequent anti-cancer therapy [baseline through study completion at up to approximately 63 months]
Time to first subsequent anti-cancer therapy will be defined as the time from treatment discontinuation for any reason to start of subsequent anti-cancer therapy or death.
- 6-month radiographic progression-free survival (rPFS) [baseline through study completion at up to approximately 63 months]
6-month radiographic progression-free survival (rPFS) will be defined as the time from enrollment to progression by by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 for measurable disease and and Prostate Cancer Working Group 3 (PCWG3) criteria for bone metastases or death, whichever occurs first.
- Overall survival [baseline through study completion at up to approximately 63 months]
Overall survival will be defined as the time from enrollment to death
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age ≥ 18 years of age
-
Metastatic disease as identified by imaging
-
Progressive mCRPC as defined by: 1) castrate levels of serum testosterone < 50 ng/dL and 2) progressive disease
-
Continued primary androgen deprivation with LHRH analogue (agonist or antagonist) if subject has not undergone bilateral orchiectomy
-
Germline testing for HSD3B1. Confirmation of positivity for the adrenal-permissive HSD3B1(1245C) allele (germline heterozygous or homozygous) will be done centrally
-
For abiraterone-progressing cohort, abiraterone must be the most immediate preceding line of therapy
-
Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
-
Adequate organ and marrow function
Exclusion Criteria:
-
Significant small cell or neuroendocrine component or histology
-
Prior enzalutamide, apalutamide, or darolutamide exposure for either hormone sensitive or CRPC. Prior abiraterone is prohibited for the abiraterone-naïve combination cohort
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Prior BTK inhibitor treatment
-
Need for concurrent CYP3A inducers and inhibitors
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Any condition including the presence of laboratory abnormalities that places the patient at unacceptable risk if the patient was to participate in the study
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Corrected QT interval calculated by the Fridericia formula per electrocardiogram within 14 days before Cycle 1 Day 1
-
Any uncontrolled active systemic infection including any infection requiring systemic IV treatment that was completed ≤ 7 days before Cycle 1 Day 1, including active infection with COVID-19, defined as 10 days from the end of COVID-19 symptoms
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Have human immunodeficiency virus (HIV) infection, human T-cell leukemia virus type 1 (HTLV1) infection, or hepatitis B virus (HBV) or hepatitis C virus (HCV) viremia or are at risk for HBV reactivation (at risk for HBV reactivation is defined as being HBs antigen positive, or anti-HBc-antibody positive), or are positive for HBV deoxyribonucleic acid (DNA). HCV ribonucleic acid (RNA) must be undetectable by laboratory test
-
Imminent or established spinal cord compression based on clinical and/or imaging findings
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Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery and stable for at least 4 weeks prior to Cycle 1 Day 1
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Major surgery within 4 weeks before Cycle 1 Day 1. Minor surgeries within 10 days before Cycle 1 Day 1. Subjects must have complete wound healing from major surgery or minor surgery before first dose of study treatment. Subjects with clinically relevant ongoing complications from prior surgery are not eligible
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Radiation therapy within 2 weeks before Cycle 1 Day
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Participation in another investigational trial and received treatment within 4 weeks before Cycle 1 Day 1
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Any other active malignancy at the time of first dose of study treatment or diagnosis of another malignancy within 2 years prior to Cycle 1 Day 1 that requires active treatment, except locally curable cancers
-
Unable to swallow tablets/capsules whole
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | UCSD Moores Cancer Center | La Jolla | California | United States | 92037 |
Sponsors and Collaborators
- Sorrento Therapeutics, Inc.
Investigators
- Study Director: Mike Royal, MD, Sorrento Therapeutics, Inc.
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- ABV-RPC-201