DIETHYLSTILBESTROL
Pre-LaunchNDAVAGINALSUPPOSITORY
Lifecycle
Pre-Launch
Clinical Trials
3
Data completeness
1/8 — Limited
Drug data last refreshed 20h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Diethylstilbestrol (DES) is a synthetic nonsteroidal estrogen delivered as a vaginal suppository, currently in pre-launch development by Eli Lilly. The mechanism of action and specific therapeutic indications are not disclosed in available data. This product represents a small-molecule hormone replacement or gynecological therapeutic.
Pre-Launch
Pre-launch stage offers opportunity to build foundational commercial infrastructure; team size and investment level will depend on regulatory approval timing and competitive positioning.
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.