A Phase 1/2 Study of Safety and Tolerability of MT-125 With Chemoradiation in Patients With Newly Diagnosed MGMT Methylated Glioblastoma

ConditionGlioblastoma
Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMyosin Therapeutics Inc.

About this trial

This is a Phase 1, single-arm MT-125 dose escalation study followed by a Phase 2, randomized parallel design dose expansion phase, to determine the safety and tolerability of MT-125 administered 5 consecutive days a week with 2 days off for the 6 weeks of outpatient treatment of Radiotherapy (RT) plus TMZ. Participants with newly diagnosed histologically or molecularly confirmed IDH wild type and MGMT methylated GBM will be eligible to enroll. The dose-limiting toxicity (DLT) observation window will be 6 weeks, starting with the first dose of MT-125 administration and chemoradiation. A Bayesian Optimal Interval (BOIN) adaptive trial design will be used to efficiently evaluate up to four dose levels. Secondary endpoints for this Phase 1/2 study will include determination of the MTD, the systemic PK of MT-125, and the RP2D of MT-125. Once the MTD is defined, additional participants will be enrolled as part of an expansion cohort, with a randomized parallel design, which will include up to 2 dose levels which are expected to be MTD and one dose below the MTD. Up to 36 participants will be enrolled in the study (up to 24 participants in the dose escalation phase and up to a total of 12 participants maximum per dose level for the two expansion cohorts).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years at the time of signing the informed consent form (ICF).

New Diagnosed with histologically or molecularly confirmed IDH wildtype and MGMT methylated GBM.

Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0, 1 or 2..

Hemoglobin ≥9.0 g/dL

Disqualifiers

Pregnant persons

Nursing persons

Persons of childbearing potential and persons able to father a child who are unwilling to employ adequate contraception (see Appendix 2 for highly effective forms of contraception)

Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the participant inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.

Trial design

Design model

Parallel

Treatments tested in this trial

  • MT-125

    Drug

    This is an investigational new drug under IND 170975.

Treatment groups

36 Participants
are divided into 5 treatment groups
Group A: MT-125 at 25 mgExperimental treatment 1 intervention
Group B: MT-125 at 50 mgExperimental treatment 1 intervention
Group C: MT-125 at 83.5 mgExperimental treatment 1 intervention
Group D: MT-125 at 100 mgExperimental treatment 1 intervention
Group E: MT-125 at MTD and one dose lower than MTDExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Dose Limiting Toxicity Measurement

The dose escalation portion of this study will follow a BOIN design with cohorts containing a min of 3 DLT evaluable participants. If the observed DLT rate at the current dose is ≤0.236, then the decision will be to escalate the dose to the next higher dose level; if the observed DLT rate at the current dose is \>0.359, then the decision will be to deescalate the dose to the next lower dose level; otherwise, the decision will be to stay at the current dose level.

Time frame
Day 1 through 6 weeks of treatment
2

Incidence and Severity of AEs

Incidence and Severity, attribution, grade and type of AE will be assessed based on the NCI CTCAE v5.

Time frame
Day 1 through 6 weeks of treatment

Secondary outcomes

1

Maximum Tolerated Dose

To determine the maximum tolerated dose (MTD) of MT-125

Time frame
Day 1 through Day 40
2

PK Parameters- Cmax

The time it takes for a drug to reach a maximum concentration after administration.

Time frame
Completed on study days; Day 1, Day 2, Day 5, Day 19, Day 33 and Day 40
3

PK Parameters-AUC 0-24hr

Area under the plasma concentration-time curve over the last 24 hour dosing interval.

Time frame
Completed on study days; Day 1, Day 2, Day 5, Day 19, Day 33 and Day 40
4

PK Parameters - T1/2

Time required for plasma concentrations of a drug to decrease by 50%

Time frame
Completed on study days; Day 1, Day 2, Day 5, Day 19, Day 33 and Day 40

Other outcomes

1

To obtain preliminary data on clinical efficacy measurements such as ORR

Overall Response Rate in those with Measurable disease

Time frame
Day 1 though on average one year following completion of treatment
2

Exploratory Analysis to obtain preliminary data on clinical efficacy

6 month Progression Free survival (PFS6) based on MRI imaging

Time frame
Up to 1 year following completion of treatment
3

To obtain preliminary data on clinical efficacy

Overall Survival (OS)

Time frame
Day 1 though on average one year following completion of treatment.

Sponsors and contacts

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