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

About This Program

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

Rationale when developing the program:

Given the above, we propose a novel combination - PSMA / CD3 therapeutic BiTE, which we believe will provide insights in next-generation cancer treatment.

PSMA

PSMA is a highly prostate-restricted membrane protein that expressed in almost all types of prostate cancer, which makes PSMA a potential target in local and metastatic prostate cancer. In particular, PSMA-targeting agents can be radiolabeled with diagnostic and/or therapeutic radionuclides. The end-products hold great clinical potential for the personalized management of metastatic prostate cancer. During the past few years, PSMA-specific tumor-targeting cell therapeutics are evolved so much and give a new outlook to use in the clinical settings.

PSMA: A versatile tool for prostate cancer therapy.Fig.1 PSMA: A versatile tool for prostate cancer therapy.

PSMA × CD3 in Cancer Studies

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

Ongoing Clinical Trials

Program Planning and Management

Creative Biolabs has extensive knowledge to develop 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-PSMA × 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-PSMA × 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 to advance their programs with more chance to succeed. Look forward to cooperating with you in the near future.

References

For Research Use Only | Not For Clinical Use

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