A Study to Evaluate the Safety and Efficacy of Gocatamig (MK-6070) and Ifinatamab Deruxtecan (I-DXd) in Participants With Relapsed/Refractory Extensive-Stage Small Cell Lung Cancer (MK-6070-002)
PHASE1PHASE2RECRUITING
Researchers are looking for new ways to treat people with extensive-stage small cell lung cancer (SCLC) that has relapsed or is refractory. Gocatamig is a new type of immunotherapy that uses a person's immune system to find and destroy cancer cells. Ifinatamab deruxtecan (also known as I-DXd) is a drug which binds to a specific target on cancer cells and delivers treatment to destroy those cells.
Durvalumab is a different type of immunotherapy that also destroys cancer cells. Researchers want to know if giving gocatamig, I-DXd, and gocatamig with I-DXd or durvalumab can treat SCLC that did not respond or stopped responding to a prior treatment. The goals of this study are to learn: * If gocatamig alone, I-DXd alone, and gocatamig with I-DXd or durvalumab are safe and well tolerated * If people who receive gocatamig alone, I-DXd alone, and gocatamig with I-DXd or durvalumab have their SCLC get smaller or go away.
Study details:
This study will consist of two parts. Part 1 will assess the safety, tolerability, and efficacy of gocatamig and I-DXd at doses determined in study MK-6070-001 (NCT: NCT04471727). Part 2 will assess the safety and tolerability of gocatamig in participants in Japan and China.
Part 3 will assess the safety, tolerability, and efficacy of gocatamig with durvalumab.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- Has histologically or cytologically confirmed SCLC that is extensive stage (defined as Stage IV (T any, N any, M1a/b/c) following at least 1 prior line of systemic therapy that included platinum-based chemotherapy
- Must be able to provide archival tumor tissue sample or fresh biopsy tissue sample
- Human immunodeficiency virus (HIV) infected participants must have well controlled HIV on antiretroviral therapy (ART)
Exclusion criteria
- Pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedure
- History of (noninfectious) pneumonitis/interstitial lung disease (ILD) that required steroids or has current pneumonitis/ILD, and or suspected ILD/pneumonitis
- Has clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses
- Active or history of immune deficiency with the exception of HIV-infected participants with well controlled HIV on ART
- History within 6 months before the first dose of study intervention of coronary/peripheral artery bypass graft and/or any coronary/peripheral angioplasty or clinically significant cardiovascular disease such as myocardial infarction, symptomatic congestive heart failure (CHF) (New York Heart Association > class II), and/or uncontrolled cardiac arrhythmia
- History of arterial thrombosis (eg, stroke or transient ischemic attack) within 6 months before the first dose of study intervention
- Active clinically significant infection requiring systemic therapy
- History of allogeneic tissue/solid organ transplant
- History of leptomeningeal disease
- Received prior radiotherapy within 2 weeks of start of study intervention, or has radiation-related toxicities, requiring corticosteroids
- Receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of chronic immunosuppressive therapy within 7 days prior to the first dose of study intervention
- Known additional malignancy that is progressing or has required active treatment within the past 3 years
- Untreated or symptomatic brain metastases
- Active viral hepatitis, defined as hepatitis A (hepatitis A virus immunoglobulin M [IgM] positive in the setting of associated signs/symptoms), hepatitis B (hepatitis B virus surface antigen [HbsAg] positive and/or detectable hepatitis B virus [HBV] deoxyribonucleic acid [DNA]), or hepatitis C (hepatitis C virus [HCV] antibody positive and detectable HCV ribonucleic acid). Participants with HBV with undetectable viral load after treatment are eligible. Participants with HCV with undetectable virus after treatment are eligible.
- Part 1 only: Radiation therapy to the lung >30 Gy within 6 months before the start of study intervention
- Part 1 only: Abdominal radiation within 4 weeks before start of study intervention
- Part 1 only: Anticancer hormonal treatment (except luteinizing hormone-releasing hormone [LHRH]) within 2 weeks before start of study intervention
- Part 1 only: Systemic anticancer therapy (except antibody-based anticancer therapy) or investigational agents within 3 weeks or 5 half-lives, whichever is longer
- Part 1 only: Antibody-based cancer therapy within 3 weeks before start of study intervention
- Part 1 only: Chloroquine/hydroxychloroquine within 2 weeks before start of study intervention
- Part 1 only: Clinically significant corneal disease
- Part 1 only: Has other uncontrolled or significant protocol-specified cardiovascular disease
Eligibility
Age eligible for study : NA
Healthy volunteers accepted : No
Gender eligible for study: ALL
Things to know
Study dates
Study start:
Primary completion:
Study completion finish:
Study type
TREATMENT
Phase
- PHASE1PHASE2
Study ID
NCT06780137
Intervention or treatment
BIOLOGICAL: Gocatamig
BIOLOGICAL: Ifinatamab Deruxtecan (I-DXd)
BIOLOGICAL: Durvalumab
Conditions
- Small Cell Lung Cancer
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
Princess Alexandra Hospital ( Site 5300)
Select from list below to view details:
Princess Alexandra Hospital ( Site 5300)
Wooloongabba, Queensland, Australia
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Who is running the clinical trial?
MS&DL
Merck Sharp & Dohme LLC
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
| Participant Group/Arm | Intervention/Treatment |
|---|---|
EXPERIMENTAL: Part 1 Arm 1: Gocatamig and I-DXd
| Biological: Gocatamig, Biological: Ifinatamab Deruxtecan (I-DXd) |
EXPERIMENTAL: Part 1 Arm 2: Gocatamig and I-DXd
| Biological: Gocatamig, Biological: Ifinatamab Deruxtecan (I-DXd) |
EXPERIMENTAL: Part 1 Arm 3a: I-DXd Monotherapy
| Biological: Ifinatamab Deruxtecan (I-DXd) |
EXPERIMENTAL: Part 1 Arm 3b: Gocatamig and I-DXd
| Biological: Gocatamig, Biological: Ifinatamab Deruxtecan (I-DXd) |
EXPERIMENTAL: Part 2 Arm 4: Gocatamig Monotherapy in Japan
| Biological: Gocatamig |
EXPERIMENTAL: Part 2 Arm 5: Gocatamig Monotherapy in China
| Biological: Gocatamig |
EXPERIMENTAL: Part 2 Arm 6: Gocatamig
| Biological: Gocatamig |
EXPERIMENTAL: Part 3 Arm 7: Gocatamig and Durvalumab
| Biological: Gocatamig, Biological: Durvalumab |
EXPERIMENTAL: Part 2 Arm 8: Gocatamig (Alternate Presentation)
| Biological: Gocatamig |
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Who Experience an Adverse Event (AE) | An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention. The number of participants who experience an AE in the study will be presented. | Up to approximately 44 months |
| Number of Participants Who Experience One or More Dose-Limiting Toxicities (DLTs) | A DLT is defined as any drug-related adverse event (AE) observed during the DLT evaluation period that meet pre-defined DTL criteria. Toxicities will be graded using National Cancer Institute Common Terminology for Adverse Events (NCI CTCAE) version 5.0, or the American Society for Transplant and Cellular Therapy (ASTCT) criteria. The number of participants who experience at least one DLT will be presented. | Up to approximately 3 weeks |
| Number of Participants Who Discontinue Study Intervention Due to an AE | An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study intervention. The number of participants who discontinue the study intervention due to an AE in the study will be presented. | Up to approximately 44 months |
| Part 1: Objective Response Rate (ORR) | ORR is defined as the percentage of participants with Complete Response (CR: disappearance of all target lesions) or Partial Response (PR: at least a 30% decrease in the sum of diameters of target lesions) per Response Evaluation Criteria In Solid Tumors Version 1.1 (RECIST 1.1). The percentage of participants who experience CR or PR as assessed by the investigator will be presented. | Up to approximately 44 months |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Part 1, Part 2 (Arm 5 and Arm 6), and Part 3 (Arm 7): Duration of Response (DOR) | For participants who demonstrate a confirmed Complete Response (CR: disappearance of all target lesions) or Partial Response (PR: at least a 30% decrease in the sum of diameters of target lesions) per RECIST 1.1, DOR is defined as the time from first documented evidence of CR or PR until progressive disease (PD) or death. Per RECIST 1.1, PD is defined as at least a 20% increase in the sum of diameters of target lesions. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered PD. DOR as assessed by the investigator will be presented. | Up to approximately 44 months |
| Part 1, Part 2 (Arm 6), and Part 3 (Arm 7): Progression-Free Survival (PFS) | PFS is defined as the time from randomization to the first documented PD or death due to any cause, whichever occurs first as assessed by RECIST 1.1. PD is defined as ≥20% increase in the sum of diameters of target lesions. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of ≥5 mm. The appearance of one or more new lesions is also considered PD. PFS as assessed by the investigator will be presented. | Up to approximately 44 months |
| Part 2 (Arm 5 and Arm 6) and Part 3 (Arm 7): ORR | ORR is defined as the percentage of participants with Complete Response (CR: disappearance of all target lesions) or Partial Response (PR: at least a 30% decrease in the sum of diameters of target lesions) per Response Evaluation Criteria In Solid Tumors Version 1.1 (RECIST 1.1). The percentage of participants who experience CR or PR as assessed by the investigator will be presented. | Up to approximately 44 months |
| Maximum Concentration (Cmax) of gocatamig | Cmax is the maximum concentration of the study drug observed in plasma. Blood samples collected pre dose and at multiple timepoints post dose will be used to determine Cmax of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| Cmax of ifinatamab deruxtecan (I-DXd) | Cmax is the maximum concentration of the study drug observed in plasma. Blood samples collected pre dose and at multiple timepoints post dose will be used to determine Cmax of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| Cmax of Anti-B7-H3 Antibody | Cmax is the maximum concentration of the study drug observed in plasma. Blood samples collected pre dose and at multiple timepoints post dose will be used to determine Cmax of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| Cmax of Deruxtecan (DXd) | Cmax is the maximum concentration of the study drug observed in plasma. Blood samples collected pre dose and at multiple timepoints post dose will be used to determine Cmax of the drug payload deruxtecan (DXd). | At designated timepoints (up to approximately 44 months) |
| Cmax of Durvalumab | Cmax is the maximum concentration of the study drug observed in plasma. Blood samples collected pre dose and at multiple timepoints post dose will be used to determine Cmax of durvalumab. | At designated timepoints (up to approximately 44 months) |
| Time to maximum concentration (Tmax) of gocatamig | Tmax is the amount of time that a drug is present at the maximum concentration is observed in plasma. Blood samples will be collected to determine the Tmax of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| Tmax of I-DXd | Tmax is the amount of time that a drug is present at the maximum concentration is observed in plasma. Blood samples will be collected to determine the Tmax of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| Tmax of Anti-B7-H3 Antibody | Tmax is the amount of time that the drug is present at the maximum concentration is observed in plasma. Blood samples will be collected to determine the Tmax of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| Tmax of DXd | Tmax is the amount of time that the drug is present at the maximum concentration is observed in plasma. Blood samples will be collected to determine the Tmax of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Area Under the Concentration-Time Curve Over the Dosing Interval t (AUCt) of gocatamig | AUCt is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration. Blood samples will be collected to determine the AUCt of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| AUCt of I-DXd | AUCt is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration. Blood samples will be collected to determine the AUCt of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| AUCt of Anti-B7-H3 Antibody | AUCt is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration. Blood samples will be collected to determine the AUCt of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| AUCt of DXd | AUCt is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration. Blood samples will be collected to determine the AUCt of the drug payload Dxd. | At designated timepoints (up to approximately 44 months) |
| Terminal Half-Life (t1/2) of gocatamig | t½ is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak. Blood samples will be collected to determine the t1/2 of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| t1/2 of I-DXd | t½ is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak. Blood samples will be collected to determine the t1/2 of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| t1/2 of Anti-B7-H3 Antibody | t½ is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak. Blood samples will be collected to determine the t1/2 of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| t1/2 of DXd | t½ is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak. Blood samples will be collected to determine the t1/2 of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Steady State Maximum Concentration (Cmax,ss) of gocatamig | Cmax,ss is a measure of the maximum level of drug in the blood, measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Cmax,ss of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| Cmax,ss of I-DXd | Cmax,ss is a measure of the maximum level of drug in the blood, measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Cmax,ss of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| Cmax,ss of Anti-B7-H3 Antibody | Cmax,ss is a measure of the maximum level of drug in the blood, measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Cmax,ss of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| Cmax,ss of DXd | Cmax,ss is a measure of the maximum level of drug in the blood, measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Cmax,ss of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Cmax,ss of Durvalumab | Cmax,ss is a measure of the maximum level of drug in the blood, measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Cmax,ss of the durvalumab. | At designated timepoints (up to approximately 44 months) |
| Steady State Ctrough (Ctrough,ss) of gocatamig | Ctrough,ss is defined as the trough concentration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Ctrough,ss of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| Ctrough,ss of I-DXd | Ctrough,ss is defined as the trough concentration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Ctrough,ss of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| Ctrough,ss of Anti-B7-H3 Antibody | Ctrough,ss is defined as the trough concentration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Ctrough,ss of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| Ctrough,ss of DXd | Ctrough,ss is defined as the trough concentration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Ctrough,ss of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Ctrough,ss of Durvalumab | Ctrough,ss is defined as the trough concentration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Ctrough,ss of durvalumab. | At designated timepoints (up to approximately 44 months) |
| Steady State Time to Maximum Concentration (Tmax,ss) of gocatamig | Tmax,ss is the amount of time that a drug is present at the maximum concentration is observed in plasma measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Tmax,ss of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| Tmax,ss of I-DXd | Tmax,ss is the amount of time that a drug is present at the maximum concentration is observed in plasma measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Tmax,ss of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| Tmax,ss of Anti-B7-H3 Antibody | Tmax,ss is the amount of time that a drug is present at the maximum concentration is observed in plasma measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Tmax,ss of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| Tmax,ss of DXd | Tmax,ss is the amount of time that a drug is present at the maximum concentration is observed in plasma measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the Tmax,ss of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Area Under the Steady State Concentration-Time Curve Over Dosing Interval t (AUCt,ss) of gocatamig | AUCt,ss is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the AUCt,ss of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| AUCt,ss of I-DXd | AUCt,ss is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the AUCt,ss of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| AUCt,ss of Anti-B7-H3 Antibody | AUCt,ss is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the AUCt,ss of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| AUCt,ss of DXd | AUCt,ss is a measure of plasma drug concentration and time and is estimated as the area under the plot of plasma concentration against time after drug administration measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the AUCt,ss of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Steady state t1/2 (t1/2,ss) of gocatamig | t1/2,ss is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the t1/2,ss of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| t1/2,ss of I-DXd | t1/2,ss is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the t1/2,ss of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| t1/2,ss of Anti-B7-H3 Antibody | t1/2,ss is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the t1/2,ss of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| t1/2,ss of DXd | t1/2,ss is defined as the time required for plasma drug concentration of study drug to decrease by 50% from peak measured at steady state (time at which the amount of drug eliminated by the body is in equilibrium with the amount taken in). Blood samples will be collected to determine the t1/2,ss of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Accumulation Ratio (AC) of gocatamig | Blood samples will be collected to determine the AC of the drug gocatamig. | At designated timepoints (up to approximately 44 months) |
| AC of I-DXd | Blood samples will be collected to determine the AC of the drug I-DXd. | At designated timepoints (up to approximately 44 months) |
| AC of Anti-B7-H3 Antibody | Blood samples will be collected to determine the AC of the anti-B7-H3 antibody. | At designated timepoints (up to approximately 44 months) |
| AC of DXd | Blood samples will be collected to determine the AC of the drug payload DXd. | At designated timepoints (up to approximately 44 months) |
| Incidence of Anti-Drug Antibodies (ADAs) Against gocatamig | Blood samples collected at designated timepoints will be used to determine the ADA response to gocatamig. The incidence of ADAs for gocatamig will be presented. | At designated timepoints (up to approximately 44 months) |
| Incidence of ADAs Against I-DXd | Blood samples collected at designated timepoints will be used to determine the ADA response to I-DXd. The incidence of ADAs for I-DXd will be presented. | At designated timepoints (up to approximately 44 months) |
| Incidence of ADAs Against Durvalumab | Blood samples collected at designated timepoints will be used to determine the ADA response to durvalumab. The incidence of ADAs for durvalumab will be presented. | At designated timepoints (up to approximately 44 months) |
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References
Clinical Trials Gov: A Study to Evaluate the Safety and Efficacy of Gocatamig (MK-6070) and Ifinatamab Deruxtecan (I-DXd) in Participants With Relapsed/Refractory Extensive-Stage Small Cell Lung Cancer (MK-6070-002)Other trials to consider
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