Clinical trials

4

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study to Evaluate the Food Effect on RNK08954 in Healthy Participants, and the Mass Balance Study of [14C]RNK08954 in Healthy Adult Male Subjects

An Study of Orally Administered RNK08954 in Healthy Adult Subjects to Determine the Effect of Food on the Pharmacokinetics of RNK08954,Mass Balance Study of \[14C\] RNK08954 in Chinese Healthy Adult Male Subjects

Participants needed: 24
Trial details
Phase: Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: Ranok Therapeutics (Hangzhou) Co., Ltd.Updated: Jan 14, 2026Locations: 1
Eligibility criteria

Healthy, adult, male or female, 18-45 years of age, inclusive, at the screening... [+3]

Clinically significant abnormalities found in comprehensive physical examination... [+20]

Status: Recruiting

To Evaluate the Safety and Efficacy of RNK08954 in Patients With Metastatic Pancreatic Ductal Adenocarcinoma.

This is a multicenter, open-label, phase Ⅱa study to explore the safety, tolerability, and preliminary efficacy of RNK08954 in metastatic pancreatic ductal adenocarcinoma harboring a KRAS G12D mutation.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Ranok Therapeutics (Hangzhou) Co., Ltd.Updated: Dec 24, 2025Locations: 2
Eligibility criteria

The subjects voluntarily joined the study and signed the informed consent, with... [+8]

Diagnosed with other pathological types of pancreatic tumors; [+17]

Status: Recruiting

A Study of RNK08954 in Subjects With Advanced Solid Tumors With KRAS ((Kirsten Rat Sarcoma) G12D Mutation

This is a first in human (FIH), Phase 1/2 open-label multi-center, dose escalation and expansion study to evaluate the safety, tolerability and pharmacokinetics of RNK08954 to determine the optimal dose and recommended dose for expansion and evaluate clinical activity in patients with advanced solid tumors with KRAS G12D mutation. This is a 2-part study: dose exploration/indication expansion and dose optimization ( to identify a dose that preserves clinical benefit with optimal tolerability).

Participants needed: 152
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ranok Therapeutics (Hangzhou) Co., Ltd.Updated: Oct 30, 2025Locations: 6
Eligibility criteria

Must be 18 years of age or older. [+31]

Concurrent anticancer therapy [chemotherapy, monoclonal antibodies, targeted the... [+16]

Status: Recruiting

A Study of RNK05047 in Subjects With Advanced Solid Tumors/Diffuse Large B-cell Lymphoma (CHAMP-1)

This is a first in human, Phase 1/2 open-label multi-center, dose escalation and expansion study to evaluate the safety, tolerability, PK, PD and efficacy of RNK05047 when administered an intravenous (IV) infusion to subjects with advanced solid tumors, including diffuse large B-cell lymphoma (DLBCL). This is a 2-part study (dose escalation, cohort expansion) with sequential enrollment.

Participants needed: 32
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Ranok Therapeutics (Hangzhou) Co., Ltd.Updated: Mar 4, 2025Locations: 5
Eligibility criteria

Pathologically documented locally advanced or metastatic solid tumor [+9]

Concurrent anticancer therapy: Radiotherapy, chemotherapy, biological therapy, o... [+6]