Prostatic Neoplasms
Conditions
Brief summary
The purpose of this study is to determine recommended Phase 2 dose (RP2D) regimen(s) of JNJ-75229414 in Part 1 (Dose Escalation and to determine safety at the RP2D regimen(s) in Part 2 (Dose Expansion).
Interventions
DRUGJNJ-75229414
JNJ-75229414 infusion will be administered intravenously.
DRUGBridging Therapy
Bridging therapy including Anti-AR agents (example, abiraterone, enzalutamide) will be administered orally and radiotherapy, or chemotherapy (example, docetaxel) will be administered intravenously.
Sponsors
Janssen Research & Development, LLC
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histology: Metastatic CRPC (mCRPC) with histologic confirmation of adenocarcinoma. Metastatic CRPC with neuroendocrine features or mixed histology is excluded * Prior Therapy: Prior treatment with at least 1 prior novel androgen receptor AR-targeted therapy (that is, abiraterone acetate, apalutamide, enzalutamide, darolutamide), or at least 1 prior chemotherapy (example, docetaxel) * Eastern Cooperative Oncology Group (ECOG) Performance Status grade of 0 or 1 * Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 or detectable prostate-specific antigen (PSA) levels based on local laboratory results * Fertile participants must use a condom with spermicide during any sexual contact with a woman of childbearing potential, including pregnant women, from the time of signing the ICF until 1 year after receiving a JNJ-75229414 infusion. Vasectomized participants must agree to use a condom to protect any sexual partner from exposure to semen for 1 year after receiving the last dose of study drug. Contraceptive (birth control) use should be consistent with local regulations regarding the acceptable methods of contraception for those participating in clinical studies
Exclusion criteria
* Prior Grade 4 Cytokine release syndrome (CRS) or Grade 3 or Grade 4 neurotoxicity related to any T cell redirection (Bispecific cluster of differentiation \[CD 3\]) * Prior Kallikrein 2 (KLK2)-targeted therapy * Prior chimeric antigen receptor T cell (CAR-T) therapy * Receiving systemic treatment less than or equal to (\<=) 6 months prior to signing informed consent) for any invasive malignancy other than prostate cancer unless approved by the sponsor. Bisphosphonates initiated greater than or equal to (\>=) 6 weeks prior signing informed consent are allowed * Less than 2 weeks between last administration anti-androgen agents (example, abiraterone or enzalutamide), poly adenosine diphosphate-ribose polymerase (PARP) inhibitors (example, olaparib) or radiotherapy, and less than 3 weeks between last administration of cytotoxic chemotherapy (example, docetaxel), radionuclides (example, radium-223, lutetium-177-Prostate-specific membrane antigen \[PSMA\]-617) or an investigational agent, and apheresis
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Adverse Events (AEs) | Up to 15 years 9 months | An AE is any untoward medical occurrence in a participant participating in a clinical study that does not necessarily have a causal relationship with the pharmaceutical/ biological agent under study. |
| Number of Participants with AEs by Severity | Up to 15 years 9 months | Severity will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0. Severity scale ranges from Grade 1 (Mild) to Grade 5 (Death). Grade 1= Mild, Grade 2= Moderate, Grade 3= Severe, Grade 4= Life-threatening and Grade 5= Death related to adverse event. |
| Part 1: Number of Participants with Dose-limiting Toxicity (DLT) | Up to 28 days | Number of participants with DLT will be assessed. The DLTs are specific adverse events and are defined as any of the following: high grade non-hematologic toxicity, or hematologic toxicity. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Area Under Plasma Concentration Versus Time Curve from Time Zero to t Time (AUC[0-t]) of JNJ-75229414 | Up to 15 years 9 months | AUC(0-t) is the area under the plasma concentration versus time curve from time zero to 't' time. |
| Peripheral T Cell Expansion and Persistence via Monitoring Chimeric Antigen Receptor T (CAR-T) Positive Cell Counts | Up to 15 years 9 months | Peripheral T cell expansion and persistence via monitoring CAR-T positive cell counts will be reported. |
| Overall Response Rate (ORR) | Up to 15 years 9 months | ORR is defined as the percentage of participants who achieve a confirmed best overall response of Complete Response (CR) or Partial Response (PR) evaluated by an independent local radiology review based on Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Prostate Cancer Working Group 3 (PCWG3) criteria will be used to assess progressive bone metastases. |
| Disease Control Rate (DCR) | Up to 15 years 9 months | DCR is defined as the sum of CR, PR, and stable disease (SD). |
| Duration of Response (DoR) | Up to 15 years 9 months | DoR is defined as the time from the date of first documented responses until date of documented progression or death whichever comes first. |
| Time to response (TTR) | Up to 15 years 9 months | TTR defined as the time from the date of first dose of study drug to the date of first documented response. |
| Number of Participants With Presence of Anti-JNJ-75229414 Antibodies | Up to 15 years 9 months | Number of participants with antibodies to JNJ-75229414 will be reported. |
| Peripheral Blood Quantitation of Vesicular Stomatitis Virus G glycoprotein (VSV-G) Copy Numbers | Up to 15 years 9 months | Peripheral blood quantitation of VSV-G copy numbers will be reported. |
| Maximum Observe Plasma Concentration (Cmax) of JNJ-75229414 | Up to 15 years 9 months | Cmax is the maximum observed plasma concentration of JNJ-75229414. |
| Time to Reach Maximum Observed Plasma Concentration (Tmax) of JNJ-75229414 | Up to 15 years 9 months | Tmax is the actual sampling time to reach maximum observed plasma concentration of JNJ-75229414. |
Countries
United States
Contacts
STUDY_DIRECTORJanssen Research & Development, LLC Clinical Trial
Janssen Research & Development, LLC
Outcome results
None listed