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A Phase I/II, Modular, Open-Label, Multi-Centre Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of AZD9750 as Monotherapy and in Combination With Other Anticancer Agents in Participants With Metastatic Prostate Cancer (ANDROMEDA)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT07336446
Status
RECRUITING
Phase
Phase 1/2
Sponsor
AstraZeneca
Executive brief
Investment-Ready Snapshot
The ANDROMEDA trial, sponsored by AstraZeneca, is a pivotal Phase I/II study evaluating AZD9750, an innovative AR-PROTAC, for the treatment of metastatic prostate cancer. Given the increasing prevalence of prostate cancer and the limitations of current therapies, AZD9750 represents a potentially significant advancement in the therapeutic landscape. The modular design allows for flexible exploration of monotherapy and combination strategies, particularly with saruparib, a PARP inhibitor. The trial's success could position AstraZeneca favorably against competitors in the prostate cancer space, particularly those focusing on AR-targeted therapies. The estimated enrollment of 300 participants and the ongoing recruitment across multiple global sites underscore the strategic importance of this asset in AstraZeneca's oncology portfolio.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT07336446
Indication
Prostate Cancer
Modality
small molecule
Target
Androgen Receptor (AR) via Proteolysis-targeting Chimeras (PROTACs)
Intervention
AZD9750, AZD5305
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.