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DRUG CLASS:

EPCAM inhibitor

2ms
Safety and Preliminary Efficacy of BNT314 in Cancer Patients With Malignant Solid Tumors (clinicaltrials.gov)
P1, N=41, Active, not recruiting, BioNTech SE | Recruiting --> Active, not recruiting | N=103 --> 41
Enrollment closed • Enrollment change • First-in-human
2ms
Near-Infrared Photoimmunotherapy Targeting Esophagogastric Junction Adenocarcinoma With Fully Human Anti-EpCAM Antibody. (PubMed, Cancer Sci)
The fully human monoclonal antibody targeting EpCAM, adecatumumab, was conjugated with the photosensitizer IR700 at different dye-antibody ratios (DAR2, DAR4, DAR7) and tested on OE19 cells and xenograft mouse models under near-infrared light irradiation...Notable EpCAM expression and homogeneity underpin EpCAM as a promising target for NIR-PIT in EGJ adenocarcinoma. The fully human anti-EpCAM antibody may be suitable for NIR-PIT in EGJ adenocarcinoma.
Journal • IO biomarker
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HER-2 (Human epidermal growth factor receptor 2)
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adecatumumab (MT201)
2ms
Phase 1 Study Evaluating BA3182 in Patients With Advanced Adenocarcinoma. (clinicaltrials.gov)
P1, N=168, Recruiting, BioAtla, Inc. | Trial completion date: Dec 2025 --> Sep 2028 | Trial primary completion date: Jun 2025 --> Sep 2028
Trial completion date • Trial primary completion date
4ms
Removal of EpCAM-positive tumor cells during intraoperative blood salvage- A pivotal multicenter clinical study (REMOVE). (PubMed, J Clin Anesth)
The study demonstrates the efficacy, safety and feasibility of CATUVAB® for the re-infusion of autologous EC processed by a cell salvage device during high-blood-loss cancer surgeries. These promising results have the potential to re-define the intraoperative blood salvage protocols in cancer surgeries.
Journal
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IL6 (Interleukin 6) • CXCL8 (Chemokine (C-X-C motif) ligand 8)
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Removab (catumaxomab)
4ms
EpCAM-targeted near-infrared photoimmunotherapy (NIR-PIT) for the treatment of breast cancer. (PubMed, Ann Med)
We first evaluated the target cell-killing efficacy of EpCAM-targeted NIR-PIT (EpCAM-NIR-PIT) using the antibody Edrecolomab in human breast and colon cancer models characterized by high EpCAM expression...Furthermore, mice that achieved CR demonstrated resistance to tumour rechallenge, indicating the establishment of long-term anticancer immunity. This study demonstrated that EpCAM-NIR-PIT, particularly when combined with immune-activating agents such as anti-PD-1, is a promising new approach for cancer treatment, inducing durable and systemic anticancer immunity.
Journal • PD(L)-1 Biomarker • IO biomarker
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EGFR (Epidermal growth factor receptor) • CD8 (cluster of differentiation 8)
4ms
A Phase Ib/II Clinical Trial of M701 in the Treatment of Malignant Pleural Effusions Caused by NSCLC (clinicaltrials.gov)
P1/2, N=96, Recruiting, Wuhan YZY Biopharma Co., Ltd. | Not yet recruiting --> Recruiting | Trial completion date: Dec 2024 --> Oct 2026 | Trial primary completion date: Jun 2024 --> Apr 2026
Enrollment open • Trial completion date • Trial primary completion date
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cisplatin • M701
4ms
Treatment of Malignant Ascites Caused by Advanced Epithelial Solid Tumors With M701 Bispecific Antibody (clinicaltrials.gov)
P3, N=312, Active, not recruiting, Wuhan YZY Biopharma Co., Ltd. | Recruiting --> Active, not recruiting | Trial primary completion date: Aug 2025 --> Nov 2025
Enrollment closed • Trial primary completion date
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M701
4ms
Treat Malignant Ascites Caused by Gastrointestinal or Ovarian Cancer With M701 Bispecific Antibody (clinicaltrials.gov)
P2, N=115, Completed, Wuhan YZY Biopharma Co., Ltd. | Active, not recruiting --> Completed | N=80 --> 115 | Trial completion date: Dec 2024 --> Aug 2024
Trial completion • Enrollment change • Trial completion date
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M701
5ms
A Study of M701 (EpCAM and CD3) in Malignant Ascites (clinicaltrials.gov)
P1, N=35, Completed, Wuhan YZY Biopharma Co., Ltd. | Recruiting --> Completed
Trial completion
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CA 19-9 (Cancer antigen 19-9)
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M701
5ms
T-cell engager toxicity in clinical phase trials; A systematic review and meta-analysis. (PubMed, Cancer Treat Rev)
Of these studies, 21 publications were included for meta-analysis, focussing on four TCEs: catumaxomab, ertumaxomab, tebentafusb, and MDX-H210. Cytokine Release Syndrome (CRS) is potentially being under-reported due to challenges of differentiation of CRS from other inflammatory mediated constituent symptoms, although Fc-independent TCEs were linked to lower inflammatory toxicity. The review highlights TCE-dependent toxicity profiles and highlights key features that may ameliorate TCE tolerance.
Retrospective data • Review • Journal
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CD40 (CD40 Molecule)
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Removab (catumaxomab) • Rexomun (ertumaxomab)