Related Experiment Video
Updated: May 3, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Preclinical Development of ONC1-13B, Novel Antiandrogen for Prostate Cancer Treatment
Alexandre V Ivachtchenko1, Oleg D Mitkin2, Elizaveta V Kudan2
11. ChemDiv Inc., 6605 Nancy Ridge Drive, San Diego, CA 92121, USA ; 2. Chemical Diversity Research Institute, 141401 Khimki, Rabochaya str, 2a-1, Moscow Reg, Russia ; 3. Alla Chem LLC., 1835 E. Hallandale Beach Blvd, #442, Hallandale Beach, FL 33009, USA.
Abstract:
Recently new drugs targeting androgen-dependent axis have been approved for the treatment of castration-resistant prostate cancer (CRPC) - Zytiga and Xtandi (formerly MDV3100), several other candidates (for example, ARN-509) are in early phases of clinical trials. However despite significant improvement in overall survival with new treatments it is evident that resistance to these drugs develops. One of the approaches to overcome it is combination therapy and from this point of view some potential for drug-drug interactions can limit the application of the drug. We describe here the preclinical development of ONC1-13B, antagonist of androgen receptor, with similar to MDV3100 and ARN-509 mechanism of action. It efficiently inhibits DHT-stimulated PSA expression and proliferation of prostate cancer cells, prevents binding of androgens to the AR ligand-binding domain, androgen-stimulated AR nuclear translocation and coactivator complex formation. In the LnCaP-Z2 xenograft model of prostate cancer ONC1-13B inhibits tumor growth and suppresses PSA expression. The in vivo activity of ONC1-13B is comparable to that of MDV3100 at similar doses, and even higher, calculated per unit of concentration in plasma. Distribution of ONC1-13B to the brain is less than that shown for MDV3100 and ARN-509, decreasing the risk of GABA-related seizure development. Additionally ONC1-13B induces significantly lower in vitro CYP3A activity than for example MDV3100 (known strong CYP3A inducer) or ARN-509 and could be well suited for co-therapy with drugs that are known CYP3A substrates. Thus ONC1-13B is a new promising antiandrogen demonstrating high efficacy in a preclinical model of prostate cancer, with lower potential for seizures and drug-drug interaction.
Insights
ONC1-13B is a new antiandrogen for castration-resistant prostate cancer (CRPC). It shows high efficacy, with reduced risks of seizures and drug interactions, making it suitable for combination therapy.
Area of Science:
- Oncology
- Pharmacology
Background:
- New drugs targeting the androgen-dependent axis have improved survival for castration-resistant prostate cancer (CRPC).
- Resistance to these treatments develops, necessitating combination therapies.
- Potential drug-drug interactions can limit the use of current CRPC therapies.
Purpose of the Study:
- To describe the preclinical development of ONC1-13B, a novel androgen receptor antagonist.
- To evaluate ONC1-13B's efficacy and safety profile compared to existing CRPC treatments.
Main Methods:
- ONC1-13B's mechanism of action was assessed in vitro, including inhibition of DHT-stimulated PSA expression and cell proliferation.
- Its ability to prevent androgen binding, nuclear translocation, and coactivator complex formation was evaluated.
- In vivo efficacy was tested in the LnCaP-Z2 xenograft model, with comparisons to MDV3100.
- Brain distribution and in vitro CYP3A activity were assessed to evaluate safety and drug-drug interaction potential.
Main Results:
- ONC1-13B demonstrated potent inhibition of prostate cancer cell growth and PSA expression, comparable or superior to MDV3100 in vivo.
- Lower brain distribution of ONC1-13B compared to MDV3100 and ARN-509 suggests a reduced risk of seizures.
- ONC1-13B induced significantly lower in vitro CYP3A activity than MDV3100 and ARN-509, indicating a lower potential for drug-drug interactions.
Conclusions:
- ONC1-13B is a promising new antiandrogen with high preclinical efficacy in prostate cancer models.
- Its favorable safety profile, including reduced seizure risk and lower drug-drug interaction potential, makes it suitable for combination therapy in CRPC treatment.
Related Concept Videos
Preclinical Development: Overview
Clinical Trials: Overview
Treatment Resistant Cancers

