Study of NGM707 As Monotherapy and in Combination with Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
- Conditions
- MesotheliomaCholangiocarcinomaNon Small Cell Lung CancerMelanomaColorectal CancerRenal Cell CarcinomaGastric CancerEsophageal CancerGlioblastomaSquamous Cell Carcinoma of Head and Neck
- Interventions
- Registration Number
- NCT04913337
- Lead Sponsor
- NGM Biopharmaceuticals, Inc
- Brief Summary
Study of NGM707 as Monotherapy and in Combination with Pembrolizumab in Advanced or Metastatic Solid Tumor Malignancies
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 179
- Histologically or cytologically documented locally advanced or metastatic solid tumor malignancy.
- Progressed or was intolerant to all available therapies known to confer clinical benefit appropriate for their tumor type, and for which the patient was eligible and willing to receive, or refused SOC treatments that are perceived to have marginal clinical benefit.
- Adequate bone marrow, kidney and liver function.
- Performance status of 0 or 1.
- Resolved acute effects of any prior therapy to baseline severity or CTCAE Grade 1 except for AEs not constituting a safety risk by Investigator judgement.
- Prior treatment targeting ILT2 and/or ILT4 or targeting HLA-G.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- FACTORIAL
- Arm && Interventions
Group Intervention Description NGM707 Monotherapy Dose Expansion Arm E NGM707 NGM707 in CRC NGM707 Combination Dose Expansion Arm B NGM707 plus pembrolizumab (KEYTRUDA®) NGM707 with pembrolizumab (KEYTRUDA®) in Non-Squamous NSCLC NGM707 Combination Dose Finding with pembrolizumab (KEYTRUDA®) NGM707 plus pembrolizumab (KEYTRUDA®) Part 1b NGM707 plus pembrolizumab (KEYTRUDA®) NGM707 Combination Dose Expansion Arm C NGM707 plus pembrolizumab (KEYTRUDA®) NGM707 with pembrolizumab (KEYTRUDA®) in SCCHN NGM707 Monotherapy Dose Expansion Arm D NGM707 NGM707 in RCC NGM707 Monotherapy Dose Escalation NGM707 Part 1a Single Agent Dose Escalation NGM707 Combination Dose Expansion Arm A NGM707 plus pembrolizumab (KEYTRUDA®) NGM707 with pembrolizumab (KEYTRUDA®) in Squamous NSCLC NGM707 Monotherapy Dose Expansion Arm F NGM707 NGM707 in Ovarian
- Primary Outcome Measures
Name Time Method Number of Patients with Clinically Significant Laboratory Abnormalities Baseline up to Approximately 24 Months Number of patients with clinically significant change from baseline in laboratory abnormalities as characterized by type, frequency, severity (graded by CTCAE version 5.0) and timing.
Number of Patients with Dose-limiting Toxicities Baseline up to 28 Days A DLT is defined as an AE that meets at least one of the criteria listed in protocol, according to National Cancer Institute (NCI) common terminology criteria for AE (CTCAE) version 5.0, and is considered by the investigator to be clinically relevant and attributed to the study treatment during the first 28 days after the first dose of study treatment.
Progression-free Survival for Patients in Expansion Cohorts Baseline up to approximately 24 months Progression-free survival is defined as the time from start of study treatment to the date of first documentation of objective tumor progression on or following study therapy per RECIST v1.1, or to death due to any cause, whichever comes first.
Duration of Response for Patients in Expansion Cohorts Baseline up to approximately 24 months Duration of Response is defined as the time from the first documentation of objective response (CR or PR) that is subsequently confirmed per RECIST v1.1, to the time of the first documentation of objective tumor progression or to death due to any cause, whichever occurs first.
Incidence of Adverse Events Baseline up to Approximately 24 Months Number of patients with adverse events (AEs) according to severity, seriousness, and relationship to study drug
An AE is defined as any untoward medical occurrence in a participant, temporally associated with the use of study treatment, whether or not considered related to the study treatment. The number of patients who experience at least one AE will be presented.Number of Patients in Expansion Cohorts with Objective Responses Baseline up to approximately 24 months Objective Response Rate is defined as the proportion of patients who achieve a confirmed complete response (CR) or partial response (PR) according to RECIST v1.1
Overall Survival for Patients in Combination Dose Expansion Cohorts Up to approximately 48 months Overall survival is defined as the date from start of the study treatment to the date of death due to any cause.
- Secondary Outcome Measures
Name Time Method Observed Plasma Concentration of NGM707 (Including Cmax) Baseline up to approximately 24 months Will be measured on Day 1, 2, 4, 8 and 15 of Cycles 1 and 3, Day 1 of Cycle 2 and Day 1 of Cycle 4 and each cycle thereafter.
Area Under the Curve (AUC) of Plasma NGM707 Baseline up to approximately 24 months Area under the curve from time zero extrapolated to the last quantifiable dose of NGM707. Time zero extrapolated to the last quantifiable time point prior to the next dose. Will be measured on Day 1, 2, 4, 8 and 15 of Cycles 1 and 3, Day 1 of Cycle 2 and Day 1 of Cycle 4 and each cycle thereafter.
Plasma Half-life (t1/2) of NGM707 Baseline up to approximately 24 months Plasma decay half-life is the time measured for the plasma concentration to decrease by one half. Will be measured on Day 1, 2, 4, 8 and 15 of Cycles 1 and 3, Day 1 of Cycle 2 and Day 1 of Cycle 4 and each cycle thereafter.
Anti-drug Antibodies (ADA) Against NGM707 Baseline up to approximately 24 months Incidence and titers of anti-drug antibodies (ADA) against NGM707. Will be measured on Day 1 of each cycle.
Trial Locations
- Locations (1)
NGM Clinical Study Site
🇨🇳Taipei, Taiwan