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

Official title

A Phase 1/Phase 2 Study to Investigate Safety, Tolerability and Efficacy With TG01/QS-21 Vaccine Administration in Patients With Confirmed KRAS or NRAS Codon 12/13 Mutation and High-risk Smoldering Multiple Myeloma or Multiple Myeloma and Evidence of Measurable Disease ≥ 1 Line of Treatment

Overview

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.

Interventions

• Biological TG01
  All participants will receive the same treatment as described under arm

Primary outcome measures

• Percentage of participants with adverse events (AEs) [Time frame: Baseline until 30 days after last dose of study drug, up to approximately 3 years]
• Percentage of participants discontinuing treatment secondary to treatment-related adverse events [Time frame: Up to approximately 3 years]

Secondary outcome measures (5)

• Number of patients with Progression Free Survival (PFS) [Time frame: Baseline to 11 years]
• Concentration of TG01-specific T-cell specific cytokine production [Time frame: Baseline until end of study, assessed up to 11 years]
• Overall response rate per patient [Time frame: Baseline to approximately 3 years]
• Overall Survival (OS) per patient [Time frame: Baseline until the end of study, assessed up to 11 years]
• Time to next treatment (TTNT) per patient [Time frame: Baseline until the end of study, assessed up to 11 years]

Eligibility criteria

Inclusion criteria

• Male or female patients ≥ 18 years of age
• RAS mutation (KRAS/NRAS codon 12/13 mutation) detected on archival or fresh bone marrow material with VariantPlex Myeloid Panel
• Confirmed diagnosis of high-risk smoldering multiple myeloma (SMM) according to IMWG criteria (30) and high-risk criteria as listed up below OR confirmed diagnosis of multiple myeloma (MM) according to IMWG criteria and measurable disease following ≥

1 line of treatment

• In patients with high-risk SMM at least 2 of 3 following abnormalities, based on laboratory data obtained at screening must be fulfilled:

• Serum M-protein >20 g/L.
• Serum involved/uninvolved FLC ratio >20.
• BMPC >20%. OR presence of ≥10% BMPC and at least one of the following based on laboratory data obtained at screening:

• Serum M-protein ≥30 g/L (If IgA, IgA ≥20g/L)
• Serum involved/uninvolved FLC ratio ≥8 (but <100)
• Abnormal PC immunophenotype (≥95% of BMPCs are clonal) and reduction of ≥1uninvolved Ig isotype (Only IgG, IgA and IgM will be considered)
• Progressive increase in Serum M-protein level (evolving type of SMM) defined as an increase of Serum M-protein ≥10% in the last 12 months before enrolment in the study. This increase must be consistent from one to another sample (i.e., no decrease observed between 2 increased Serum M-protein values)
• Both high-risk SMM and MM patients must have evidence of measurable disease in accordance with IMWG criteria
• If patient with MM was eligible for ASCT, ASCT must have been performed, and patients cannot be enrolled until 3 months after ASCT
• Patient should not be expected to require immediate, subsequent line of treatment for at least 2 months
• Patient has not had reduction of clonal plasma cell markers for last two cycles (last two months if off treatment). If a patient had no reduction during the last two cycles of induction before ASCT, the patient can be enrolled, provided 3 months after ASCT
• Following ASCT, the patient cannot be enrolled without having tried lenalidomide maintenance given at standard doses for at least two cycles, if the clonal markers had a reduction during the last 2 cycles of induction treatment. Lenalidomide will be stopped when entering the study
• ECOG performance status 0-1
• Female patients of child-bearing potential (FCBP) must have negative serum pregnancy test at Screening and agree to use a highly effective method of contraception during treatment and for 3 months following last dose of drug.
• Male patients must use an effective barrier method of contraception during treatment and for 3 months following the last dose if sexually active with a FCBP.
• Ability to provide written informed consent and can understand and comply with the requirements of the study

Exclusion criteria

• Pregnant or lactating women or women without a pregnancy test at baseline (postmenopausal women must have been amenorrhoeic for at least 12 months to be considered of non-childbearing potential)
• Medical conditions such as but not limited to:

• Any uncontrolled infection
• Uncontrolled cardiac failure classification III or IV (NYHA)
• Uncontrolled systemic and gastro-intestinal inflammatory conditions
• History of adverse reactions to vaccines
• Active malignancy with worse prognosis than multiple myeloma
• Likely to require treatment intervention for multiple myeloma within two months of start of treatment with TG01/QS-21
• Known history of positive tests for HIV/AIDS, hepatitis B or C
• Planned to receive yellow fever or other live (attenuated) vaccines during the course of study
• Known hypersensitivity to QS-21.
• Only participants who are able to consent will be included in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

Norway · 1 center

• Oslo Myeloma Center — Oslo

Identifiers

NCT: NCT05841550 · OMC04

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗