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Updated: Jun 3, 2026

Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
An antibody-cytotoxic conjugate, BIIB015, is a new targeted therapy for Cripto positive tumours
Rebecca K Kelly1, Dian L Olson, Yaping Sun
1Biogen Idec, Inc, Discovery Oncology, 14 Cambridge Center, Cambridge, MA 02142, USA.
Abstract:
BIIB015 is an immunoconjugate created for the treatment of solid tumours and is currently in Phase I of clinical evaluation. BIIB015 consists of a humanised monoclonal antibody against the Cripto protein carrying a payload, via a hindered disulphide linker, of the maytansinoid derivative, DM4. Cripto is a GPI-linked protein required for signal transduction of the TGF-beta ligand, Nodal. Cripto has been previously described as an oncogene and fits the classic pattern of an embryonic gene that is re-expressed in a transformed tumour cell. Cripto expression is highly prevalent on a number of solid tumours, including greater than 75% of breast, lung, and colorectal tumours. Our report documents for the first time that targeting the cell surface Cripto protein with an anti-Cripto antibody-cytotoxic conjugate is an effective means of inhibiting or regressing growth of Cripto positive tumours. BIIB015 which utilises a 'cleavable' linker containing a disulphide bond exhibits superior activity when compared to huB3F6 mAb conjugates with different linker systems, including one with a 'non-cleavable' linker. BIIB015 displays specificity for Cripto in both in vitro and in vivo experiments. In human xenograft models originating from lung (Calu-6), colon (CT-3), testicular (NCCIT) and breast (MDA-MB-231) tumour samples, BIIB015 shows robust activity with results ranging from >50% tumour inhibition to complete tumour regression. The efficacy seen in the MDA-MB-231 model, a triple negative (-HER2, -ER, and -PR) tumour, is particularly exciting since there is currently no approved therapy for this indication. In addition, BIIB015 can be combined with standard of care chemotherapeutics for enhanced efficacy.
Insights
BIIB015, an antibody-drug conjugate targeting the Cripto oncogene, effectively inhibits solid tumor growth. This novel immunoconjugate shows promise in preclinical models, including triple-negative breast cancer.
Area of Science:
- Oncology
- Immunotherapy
- Drug Development
Background:
- Cripto is an oncogene re-expressed in various solid tumors, including breast, lung, and colorectal cancers.
- Targeting Cripto presents a potential therapeutic strategy for cancers with high Cripto expression.
- Current treatments for triple-negative breast cancer are limited.
Purpose of the Study:
- To evaluate the efficacy of BIIB015, an anti-Cripto immunoconjugate, in treating solid tumors.
- To compare the activity of BIIB015 with different linker systems.
- To assess the potential of BIIB015 in combination therapy.
Main Methods:
- BIIB015 is an immunoconjugate comprising a humanized anti-Cripto antibody linked to DM4 maytansinoid.
- In vitro and in vivo studies were conducted using human xenograft models (lung, colon, testicular, breast).
- Comparative analysis of BIIB015 with different linker systems (cleavable vs. non-cleavable).
Main Results:
- BIIB015 demonstrated specific binding to Cripto and potent anti-tumor activity in preclinical models.
- Significant tumor inhibition and complete regression were observed in xenograft models.
- BIIB015 with a cleavable linker showed superior activity compared to non-cleavable linker conjugates.
- Remarkable efficacy was noted in the MDA-MB-231 triple-negative breast cancer model.
Conclusions:
- Targeting cell surface Cripto protein with BIIB015 is an effective strategy for inhibiting or regressing Cripto-positive solid tumors.
- BIIB015 exhibits robust anti-tumor activity and specificity in preclinical settings.
- BIIB015 holds promise as a therapeutic agent, particularly for triple-negative breast cancer, and can be combined with chemotherapy.
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