drugset / Trial / NCT05841550

The TG01 Study With TG01/QS-21 Vaccine in Patients With High-risk Smouldering Multiple Myeloma and Multiple Myeloma

NCT05841550

Phase 1/2 Recruiting 20 enrolled Oslo University Hospital Targovax ASA · collab
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to test the safety, tolerability, and efficacy of TG01 vaccination in patients with KRAS or NRAS mutation on codon 12/13 mutation who has multiple myeloma or high-risk smoldering multiple myeloma. The main question it aims to answer are: Is TG01/QS-21 vaccination safe and tolerable for this patient group? Is TG01/QS-21 vaccination treatment efficient in this group in terms of increased overall response rate, overall survival rate, progression-free survival, and time til next treatment? Is there an immunological response to the vaccine? Participants will be given TG01/QS-21 vaccination treatment. Treatment consists of 12 doses of TG01/QS-21 vaccine given every two weeks in the first 12 weeks, followed by every eight weeks until week 52.

Timeline

Start
2023-05-19
Primary completion
2027-05-19
Completion
2035-05-19

Drugs

EvaluationDrugModalityDoseRoute
Subject apricoxib Small molecule 0.7 mg Subcutaneous
Background QS-21 Other / unclassified 50 ug Subcutaneous