Drug intelligence / Profile preview

pasritamig + docetaxel

Development stage
Phase 3
Lead developer
Johnson & Johnson
Modality
T-cell Engagers → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

Pasritamig + docetaxel is an investigational combination therapy being developed for the treatment of metastatic castration-resistant prostate cancer (mCRPC). Pasritamig (JNJ-78278343) is a first-in-class, bispecific T-cell-engaging antibody that targets human kallikrein 2 (KLK2), a prostate-specific antigen, and CD3 on T cells, thereby redirecting T cells to selectively destroy KLK2-expressing prostate cancer cells. Docetaxel is an established taxane chemotherapy that inhibits microtubule depolymerization, leading to cell cycle arrest and apoptosis. The combination is designed to leverage the cytotoxic effects of chemotherapy alongside targeted immunotherapy to improve outcomes in patients whose disease has progressed after treatment with an androgen receptor pathway inhibitor (ARPI). In clinical trials, the combination has demonstrated a manageable safety profile consistent with docetaxel monotherapy and encouraging clinical activity, including high rates of prostate-specific antigen (PSA) response.

Other names
JNJ-78278343 + docetaxelJNJ-78278343 plus docetaxelJNJ78278343 plus docetaxelJNJ 78278343 plus docetaxeldocetaxel + pasritamigdocetaxel plus pasritamigpasritamig + docetaxelpasritamig plus docetaxel
02

Targets

CD3 (T-cell surface glycoprotein CD3)HK2 (Hexokinase Type II)TUBB (Tubulin (alpha and beta subunits))

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