EligibleTrials

A Study of TSN1611 Treating Patients With Advanced Solid Tumors Harboring KRAS G12D Mutation

Recruiting · NCT06385925 · Interventional (participants receive a specific treatment) · Lead sponsor: Tyligand Pharmaceuticals (Suzhou) Limited

View the official record on ClinicalTrials.gov →
Lung cancerColorectal cancerPancreatic cancer

Interventions studied

TSN1611

What this trial is about

The study is a first-in-human (FIH), open-label, multi-center phase 1/2 study of TSN1611 in subjects with KRAS G12D mutant advanced solid tumors. This study will consist of a phase 1 dose escalation part and phase 2 dose expansion part. This study will evaluate the efficacy of TSN1611 at RP2D(s) through ORR using RECIST version 1.1, and determine and confirm the MTD/RP2D for TSN1611 in combination with cetuximab, in combination with cetuximab and mFOLFOX6, in combination with gemcitabine and albumin-bound paclitaxel in subjects with selected solid tumors.

Who can take part

Age range
18 Years to 75 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1, Phase 2
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

57 locations listed across 2 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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