TTrialPathMatch Me to Trials
← Back to trials
RecruitingAdvanced Solid TumorDLBCL

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

Eligible age

18+ yrs

Accepts

All genders

Locations

3 states

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

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.

Sponsor: Ranok Therapeutics (Hangzhou) Co., Ltd.

You may qualify if…

  • Pathologically documented locally advanced or metastatic solid tumor
  • Refractory or intolerant to all available standard-of-care therapies for advanced disease
  • Measurable disease
  • Archived tumor tissue collected
  • ECOG Performance Status of 0 or 1
  • BMI ≥ 18 kg/m2
  • Adequate liver, renal, hematologic, and coagulation parameters
  • Negative serum pregnancy test (for women of childbearing potential) at Screening and a negative urine or serum pregnancy test on Day 1 prior to the first infusion

You may not qualify if…

  • Concurrent anticancer therapy: Radiotherapy, chemotherapy, biological therapy, or other anticancer investigational agents NOTE: at least 5 half-lives must have been ensued for any prior systemic cancer therapy agent before subject received the study drug on Day 1
  • Unresolved toxicities from prior anticancer therapy, defined as not having resolved according to CTCAE version 5.0 Grade ≤ 1, excluding Grade 1 alopecia
  • Presence or suspicion of active central nervous system (CNS) metastases and/or leptomeningeal carcinomatosis
  • Peripheral neurotoxicity ≥ Grade 2 according to CTCAE v5.0
  • Known active infection with HIV, HTLV-1, hepatitis B or C
  • Women who are pregnant or breastfeeding
  • History of another malignancy unless the subject has been treated with curative intent for this malignancy

Where it's recruiting

Georgia

Atlanta

Kentucky

Louisville

New York

New York

Source: ClinicalTrials.gov · NCT05487170 · last updated 2025-03-04