Next-IO™ Anti-MUC16 × CD3 Therapeutic Bispecific Antibody Program

About This Program

This program aims to develop anti-MUC16 × CD3 therapeutic Bispecific Antibody for immuno-oncology.

Mucin-16 (MUC16, CA125) is the largest member of the mucin family, consisting of high-molecular-weight glycoproteins synthesized by human epithelial cells to protect and heal the epithelial surface. The extracellular portion of MUC16 can be extracted and released into serum as circulating epitope, cancer antigen 125 (CA125), which is a serum biomarker for mature ovarian cancer (OC). Not only does MUC16 used in clinical diagnosis but also for the prognosis of the disease. MUC16 overexpression on the cancer cell surface is associated with poor prognosis in pancreatic cancer, colon cancer, and OC patients. In particular, MUC16 produces a key tumor-promoting effect in OC, especially on the cytoplasmic tail domain (CTD) of MUC16.

Given the reasons mentioned above, we propose a novel combination- MUC16 / CD3 therapeutic BiTE, of which we believe will provide insights for the next-generation cancer treatment.

MUC16

MUC16 is a high-molecular-weight type I transmembrane glycoprotein containing more than 22,000 amino acids. It is made up of an extracellular N-terminal region, in which the heavy glycosylation region is interspersed with sea urchin sperm protein, enterokinase and agrin (SEA); a transmembrane region; and a 32 amino acid short cytoplasmic tail region (CTD).

Highlighted Functions:

  • MUC16 is overexpressed in patients with breast, ovarian and pancreatic tumors and weighs heavily in the disease progression and metastasis.
  • After MUC16 cleaves from the cell surface and enters the circulation. The circulating MUC16 levels play a key role in the ability of cancer cells to evade the host immune system and prevents anti-MUC16-targeted drugs from reaching the tumor area.
  • Antibodies that target MUC16 cab elicit T cell and B cell responses in patients, making them promise candidates in vaccine developments.
  • The carboxy terminus of MUC16 acts as an oncogene, meaning it can induce signaling events leads to tumor progression.

Mesothelin binding to CA125/MUC16 promotes pancreatic cancer.Fig.1 Mesothelin binding to CA125/MUC16 promotes pancreatic cancer.

In summary, the emergence of novel MUC16 antigen as a potential target for T cell-redirected antibody (TRAB) therapy has brought hope to the development of future immunotherapeutic strategies.

MUC16 × CD3 in Cancer Studies

Here are some published data about MUC16 × CD3 working as a potential target for cancer immunotherapy.

Ongoing Clinical Trials

Program Planning and Management

Creative Biolabs has extensive knowledge of end-to-end program development. For each program, we are committed to delivering the final complete program to our clients within 1.5 years before entering the IND stage.

Anti-MUC16 × CD3 Therapeutic Bispecific Antibody Program

Cooperation

Creative Biolabs is looking for potential partners (include but not limit to major pharma or biotech firms) to develop anti-MUC16 × CD3 therapeutic Bispecific Antibody program together. Our scientists are dedicated to bringing years of valuable experience to our partner and achieve a meaningful partnership together. For any partners interested in our Next-IO™ programs, Creative Biolabs welcomes collaboration.

Here are two ways for your choice, and please contact us for more details.

1) Collaborate with us and co-develop the programs from the discovery phase to IND enabling. Costs will be shared.
2) Become a licensed candidate for our programs.

With our quality control protocol and knowledge of global regulatory requirements, we can help our partners advance their programs with more chance to succeed. Look forward to cooperating with you in the near future.

References

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