DIETHYLSTILBESTROL
Pre-LaunchNDAVAGINALSUPPOSITORY
Lifecycle
Pre-Launch
Clinical Trials
3
Data completeness
1/8 — Limited
Drug data last refreshed 17h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Diethylstilbestrol (DES) is a synthetic estrogen small molecule administered as a vaginal suppository. This product is in pre-launch stage under NDA sponsorship by Eli Lilly and Company. The specific indication and mechanism of action require clarification from current clinical data.
Pre-Launch
As a pre-launch product with no commercial data, the team is likely focused on launch preparation, regulatory strategy, and market access planning with smaller core commercial staffing than established brands.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
A Study of Pharmacodynamic and Genetic Parameters of Abira-DES Study Participants (NCT02217566) - Participants With Metastatic Castration-Resistant Prostate Cancer Treated With Abiraterone Acetate Following Unresponsive Treatment With Diethylstilbestrol
Started Mar 2020
42 enrolled
Metastatic Castration-resistant Prostate Cancer
Study of Abiraterone Acetate in Participants With Metastatic Castration-Resistant Prostate Cancer (mCRPC), Chemo-Naive, Who Received a Prior Diethylstilbestrol Therapy
Started Sep 2014
46 enrolled
Prostatic Neoplasms
Docetaxel and Diethylstilbestrol in the Treatment of Androgen Independent Prostate Cancer
Started Dec 2002
30 enrolled
Prostate Cancer
Career Relevance
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.