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Updated: Apr 24, 2026

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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ODM-201 is safe and active in metastatic castration-resistant prostate cancer
Cancer Discovery
|September 4, 2014
Abstract:
The next-generation AR inhibitor ODM-201 is tolerable and induces PSA responses in metastatic CRPC.
Insights
The novel androgen receptor inhibitor ODM-201 is well-tolerated and effectively lowers prostate-specific antigen levels in patients with metastatic castration-resistant prostate cancer.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic castration-resistant prostate cancer (mCRPC) remains a significant clinical challenge.
- Androgen receptor (AR) signaling is a key driver in prostate cancer progression.
Purpose of the Study:
- To evaluate the tolerability and efficacy of ODM-201, a next-generation AR inhibitor, in patients with mCRPC.
Main Methods:
- Clinical trial evaluating ODM-201 in mCRPC patients.
- Assessment of drug tolerability and prostate-specific antigen (PSA) response.
Main Results:
- ODM-201 demonstrated a tolerable safety profile.
- Treatment with ODM-201 induced significant PSA responses, indicating anti-tumor activity.
Conclusions:
- ODM-201 is a promising therapeutic option for mCRPC.
- The observed PSA responses suggest clinical benefit in this patient population.

