Skip to main content

Newly reported results

Setidegrasib (ASP3082) — KRAS G12D targeted protein degrader (phase I)

A Study of ASP3082 in Adults With Advanced Solid Tumors

Phase
Phase I
Recruitment
Recruiting
Results maturity
Interim analysis
Publication
Peer-reviewed
Regulatory approval
No regulatory approval
NCT
NCT05382559
Registry checked
2026-10-29
Editorial update
2026-10-29

Not a treatment recommendation. Experimental or ongoing research does not by itself replace standard care.

For patients

What is being studied? An early clinical study tested a new drug that tries to destroy the harmful KRAS G12D protein in cancer cells. It is not standard care yet.

Why promising? First-in-class KRAS G12D degrader; provides a clinical signal for a major unmet need in pancreas cancer.

What is not proven? Approval; randomized superiority; long-term OS; class comparison versus MRTX1133.

Is this standard care today? This listing alone does not replace standard care; approval and guideline context require clinician judgment.

For clinicians

NCT05382559; NEJM 2026. NSCLC ORR ~36%, PDAC ORR ~24% (600 mg). Infusion reactions common. Numeric summary pending clinician review.

Cancer / population: Pancreas, Multiple / solid tumors — Önceden tedavi almış ileri solid tümörler (KRAS G12D); NSCLC ve PDAC alt analizleri

Intervention: Setidegrasib (IV, haftalık; RP2D 600 mg kohortları)

Primary endpoint: Güvenlik / DLTs / faz II doz

Source-verified summary: NEJM 2026: 600 mg cohort — NSCLC ORR 36% (n=45); metastatic PDAC ORR 24% (n=21), mPFS 3.0 mo, mOS 10.3 mo. Not registrational.

Limitations: Faz I; seçilmiş kohort; standart bakım değildir.

Related research area

Sources

← Back to explorer