This Target Evaluation Report for CCND1 is generated from PatSnap Life Sciences MCP data workflows, combining Target & Disease MCP biology context with Clinical Trials MCP validation and competitive signals.
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21 Direct drug records from Target & Disease MCP | 15 Development records in target context | 15 Disease associations captured | 2 Clinical trial records from Clinical Trials MCP |
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Target & Disease MCP profiles CCND1/cyclin D1 as the regulatory component of cyclin D1-CDK4 complexes that phosphorylate RB-family proteins, release E2F transcription, and integrate mitogenic and antimitogenic signals during G1/S progression.
The MCP workflow retrieved 21 direct drug records, 15 development records, and 15 disease associations. Clinical Trials MCP returned only 2 direct trial records, suggesting that CCND1 is more often used as a biomarker or pathway node than as a direct drug target.
The direct trial sample includes briciclib in advanced solid tumors and ON 013105 in lymphoma/acute lymphoid leukemia, both terminated Phase 1 studies. That makes direct CCND1 intervention high-risk without a new modality or biomarker thesis.
CCND1 IP should be tied to amplification, mantle-cell lymphoma biology, pathway diagnostics, or synthetic-lethal combinations rather than direct cyclin inhibition alone.
Clinical Trials MCP returned 2 registered trial records connected to CCND1. The sample below is used as a directional competitive readout rather than a full regulatory review.
| Trial | Phase | Status |
|---|---|---|
| Briciclib dose-escalation, safety, and pharmacokinetic study in advanced solid tumors | Phase 1 | Terminated |
| ON 013105 safety study in lymphoma and acute lymphoid leukemia | Phase 1 | Terminated |
CCND1 is better treated as a pathway biomarker and patient-selection variable unless a program has a credible direct-modulation technology or synthetic-lethal strategy.
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