A Study of JNJ-69086420, an Actinium-225-Labeled Antibody Targeting Human Kallikrein-2 (hK2) for Advanced Prostate Cancer

Clinicaltrials.gov ID: NCT04644770
db-list-check Status RECRUITING
b-loader Phase PHASE1
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 111

Conditions

Prostatic Neoplasms, Adenocarcinoma

Drugs

JNJ-69086420

Summary

The purpose of this study is to determine the recommended Phase 2 dose(s) (RP2D[s]) of JNJ-69086420 in Part 1 (Dose Escalation) and to determine safety and preliminary signs of clinical activity at the RP2D(s) in Part 2 (Dose Expansion).

Locations

7 locations Found with status Recruiting

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Status

  • RECRUITING

Central Contacts

Study Director

  • Janssen Research & Development, LLC Clinical Trial

Eligibility Criteria

Inclusion Criteria:

* Metastatic castration resistant prostate cancer (mCRPC) with histologic confirmation of adenocarcinoma (adenocarcinoma with small-cell or neuroendocrine features is allowed) with prior exposure to at least one androgen receptor (AR) targeted therapy (example, abiraterone acetate, enzalutamide, apalutamide, darolutamide). In addition: Part 1: prior taxane or other chemotherapy is acceptable but not required. Part 2a: prior taxane or other chemotherapy required, Part 2b: no prior taxane or other chemotherapy, Part 2c: mCRPC that has progressed after prior treatment with lutetium Lu-177 vipivotide tetraxetan
* Prior orchiectomy or medical castration; or, for participants who have not undergone orchiectomy, must be receiving ongoing androgen deprivation therapy with a gonadotropin releasing hormone (GnRH) analog (agonist or antagonist) prior to the first dose of study drug and must continue this therapy throughout the treatment phase
* Palliative radiotherapy (for example [eg], soft tissue lesions) must be completed greater than (>) 2 weeks prior to start of study drug except for palliative radiotherapy for pain (eg, bone pain), which may be used any time prior to first dose
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
* Adequate organ functions as reflected in laboratory parameters

Exclusion Criteria:

* Prior treatment with radium Xofigo (Ra 223 dichloride), strontium, samarium, or other radioconjugate therapy. In addition: Part 2b: Prior treatment with chemotherapy (eg, docetaxel) or poly ADP ribose polymerase (PARP) inhibitors. Part 2c: Prior treatment with lutetium Lu-177 vipivotide tetraxetan is permitted
* Known history of myelodysplastic syndrome, leukemia, or hematological malignancy with features suggestive of myelodysplastic syndrome/acute myeloid leukemia at any timepoint
* Toxicity from prior anticancer therapy has not resolved to baseline levels or to Grade less than or equal to (<=) 1 (except alopecia, radiation tissue fibrosis, or peripheral neuropathy)
* Known allergies, hypersensitivity, or intolerance to JNJ-69086420 or its excipients and protein therapeutics
* Active or chronic hepatitis B or hepatitis C infection

Study Plan

Part 1: Dose Escalation

EXPERIMENTAL

Participants will receive intravenous (IV) injection of JNJ-69086420 with one or multiple doses. The dose levels will be escalated based on the dose limiting toxicities (DLT) evaluation by Study Evaluation Team (SET) until the recommended Phase 2 Dose (RP2D) has been identified.

  • DRUG:

    JNJ-69086420

    Description:

    Participants will receive IV injection of JNJ-69086420.

Part 2: Dose Expansion

EXPERIMENTAL

Participants in one or more cohorts will receive intravenous (IV) injection of JNJ-69086420 at the RP2D(s) determined in Part 1.

  • DRUG:

    JNJ-69086420

    Description:

    Participants will receive IV injection of JNJ-69086420.

Outcome Measures

Primary Outcome Measures

Part 1 and Part 2: Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability

Time Frame: Up to 2 years and 4 months

Part 1: Number of Participants with Dose-Limiting Toxicity (DLT)

Time Frame: Up to 2 years and 4 months

Part 1 and Part 2: Number of Participants with AEs by Severity

Time Frame: Up to 2 years and 4 months

Secondary Outcome Measures

Percentage of Participants with Prostate Specific Antigen (PSA) Response

Time Frame: Up to 2 years and 4 months

Overall Response Rate (ORR)

Time Frame: Up to 2 years and 4 months

Maximum Observed Serum Concentration/Radioactivity (Cmax) of JNJ-69086420

Time Frame: Up to 2 years and 4 months

Time to Reach Maximum Observed Serum Concentration/Radioactivity (Tmax) of JNJ-69086420

Time Frame: Up to 2 years and 4 months

Area Under the Serum Concentration-time Curve From Time Zero to t Time (AUC[0-t]) of JNJ-69086420

Time Frame: Up to 2 years and 4 months

Number of Participants With Anti-JNJ-69086420 Antibodies

Time Frame: Up to 2 years and 4 months

Timeline

  • Last Updated
    October 26, 2024
  • Start Date
    November 25, 2020
  • Today
    February 5, 2025
  • Completion Date ( Estimated )
    August 14, 2028

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