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NCT05156905

Study of Docetaxel Combined with Cirmtuzumab in Metastatic Castration Resistant Prostate Cancer

Terminated Phase 1 Last updated 9 October 2024
What this trial tests

Phase 1 trial testing Cirmtuzumab in Metastatic Castration-resistant Prostate Cancer in 6 participants. Terminated before completion.

Timeline
16 June 2022
Primary endpoint
1 October 2024
1 October 2024

Quick facts

Lead sponsorUniversity of California, San Diego
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment6
Start date16 June 2022
Primary completion1 October 2024
Estimated completion1 October 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, San Diego

Who can join

18 and older, male only, with Metastatic Castration-resistant Prostate Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to examine the safety and efficacy of cirmtuzumab in combination with standard of care docetaxel in patients with metastatic castration resistant prostate cancer. Docetaxel is a taxane chemotherapy which has been shown to prolong survival in men with castration resistant prostate cancer. Cirmtuzumab is a monoclonal antibody that targets the receptor called ROR1 of the non-canonical Wnt pathway and is suspected to contribute to prostate cancer growth and progression.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Wnt/β-catenin signaling pathway in carcinogenesis and cancer therapy.
    Song P, Gao Z, Bao Y, Chen L, et al · · 2024 · cited 208× · PMID 38886806 · DOI 10.1186/s13045-024-01563-4
  2. Signaling pathways in the regulation of cancer stem cells and associated targeted therapy.
    Manni W, Min W. · · 2022 · cited 52× · PMID 36226253 · DOI 10.1002/mco2.176
  3. Wnt signaling in cancer: from biomarkers to targeted therapies and clinical translation.
    Tufail M, Jiang CH, Li N. · · 2025 · cited 36× · PMID 40170063 · DOI 10.1186/s12943-025-02306-w
  4. Exploring the Wnt Pathway as a Therapeutic Target for Prostate Cancer.
    Koushyar S, Meniel VS, Phesse TJ, Pearson HB. · · 2022 · cited 33× · PMID 35204808 · DOI 10.3390/biom12020309
  5. Profiling and targeting cancer stem cell signaling pathways for cancer therapeutics.
    Borlongan MC, Wang H. · · 2023 · cited 30× · PMID 37305676 · DOI 10.3389/fcell.2023.1125174
  6. Targeting ligand-dependent wnt pathway dysregulation in gastrointestinal cancers through porcupine inhibition.
    Flanagan DJ, Woodcock SA, Phillips C, Eagle C, et al · · 2022 · cited 26× · PMID 35358569 · DOI 10.1016/j.pharmthera.2022.108179
  7. Crosstalk between Wnt/β-catenin signaling pathway and DNA damage response in cancer: a new direction for overcoming therapy resistance.
    Zhang X, Yu X. · · 2023 · cited 19× · PMID 37601042 · DOI 10.3389/fphar.2023.1230822
  8. High-purity CTC RNA sequencing identifies prostate cancer lineage phenotypes prognostic for clinical outcomes.
    Sharifi MN, Sperger JM, Taylor AK, Tippins KE, et al · · 2025 · cited 14× · PMID 39912912 · DOI 10.1158/2159-8290.cd-24-1509

Verify or expand the search:

Other trials of Cirmtuzumab

Trials testing the same drug.

Other recruiting trials for Metastatic Castration-resistant Prostate Cancer

Currently open trials in the same condition.

Other University of California, San Diego trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05156905.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing