M6620 First in Human Study
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| ClinicalTrials.gov Identifier: NCT02157792 |
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Recruitment Status :
Completed
First Posted : June 6, 2014
Last Update Posted : April 1, 2020
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Sponsor:
EMD Serono Research & Development Institute, Inc.
Collaborator:
Merck KGaA, Darmstadt, Germany
Information provided by (Responsible Party):
EMD Serono ( EMD Serono Research & Development Institute, Inc. )
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Brief Summary:
An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics (PK) of M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Advanced Solid Tumor | Drug: M6620 Drug: Gemcitabine Drug: Cisplatin Drug: Etoposide Drug: Carboplatin Drug: Irinotecan | Phase 1 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 200 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics of VX-970/M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors |
| Actual Study Start Date : | December 10, 2012 |
| Actual Primary Completion Date : | March 11, 2020 |
| Actual Study Completion Date : | March 11, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Part A
This part will be 3 + 3 dose escalation study of M6620 in combination with gemcitabine as well as gemcitabine and cisplatin in participants with advanced solid tumors.
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Drug: M6620
Other Name: VX-970 Drug: Gemcitabine Drug: Cisplatin |
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Experimental: Part B
This part will be 3 + 3 dose escalation study of M6620 in combination with cisplatin or cisplatin and etoposide in participants with advanced solid tumors.
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Drug: M6620
Other Name: VX-970 Drug: Cisplatin Drug: Etoposide |
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Experimental: Part B2
This part will be 3 + 3 dose escalation study of M6620 in combination with irinotecan in participants with advanced solid tumors.
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Drug: M6620
Other Name: VX-970 Drug: Irinotecan |
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Experimental: Part C1
This will be the expansion part of the study in which participants with advanced non-small cell lung cancer (NSCLC) will be administered M6620 in combination with gemcitabine.
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Drug: M6620
Other Name: VX-970 Drug: Gemcitabine |
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Experimental: Part C2
This will be the expansion part of the study in which participants with advanced triple negative breast cancer (TNBC) will be administered M6620 in combination with cisplatin.
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Drug: M6620
Other Name: VX-970 Drug: Cisplatin |
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Experimental: Part C3
This will be the expansion part of the study in which participants with platinum-resistant advanced small cell lung cancer (SCLC) will be administered M6620 in combination with cisplatin or carboplatin.
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Drug: M6620
Other Name: VX-970 Drug: Cisplatin Drug: Carboplatin |
Primary Outcome Measures :
- Parts A, B, B2, C1, C2, C3: Safety parameters, including adverse event (AEs), clinical laboratory values (serum chemistry, hematology, and urinalysis), vital signs, and electrocardiogram (ECG) assessments [ Time Frame: Screening through Safety Follow-up (approximately 22 weeks) ]
- Parts C1, C2, C3: Overall Response Rate (ORR) for all participants in Part C1 (NSCLC), ORR for participants in Part C2 (TNBC) who are basaloid subtype and BRCA1/BRCA2 germline wild-type, ORR for all participants in Part C3 (SCLC) [ Time Frame: 1 year ]
Secondary Outcome Measures :
- Part A: Maximum tolerated dose (MTD) of M6620 administered in combination with cisplatin and gemcitabine and in combination with gemcitabine [ Time Frame: 1 year ]
- Part A: Pharmacokinetic (PK) parameter estimates of M6620 in combination with cisplatin and gemcitabine and in combination with gemcitabine [ Time Frame: 1 year ]
- Part B, B2: Maximum tolerated dose (MTD) of M6620 in combination with cisplatin or cisplatin and etoposide or irinotecan [ Time Frame: 1 year ]
- Part B, B2: PK parameter estimates of M6620 in combination with cisplatin or cisplatin and etoposide or irinotecan [ Time Frame: 1 year ]
- Part B: PK parameter estimates of etoposide derived from plasma concentration-time data after coadministration with M6620 and in the absence of M6620 [ Time Frame: 1 year ]
- Parts A, B, B2: Objective tumor response (OR) as evaluated by Response Criteria Evaluation in Solid Tumors (RECIST) 1.1 [ Time Frame: 1 year ]
- Part C2: Overall Response Rate in all participants in Part C2 [ Time Frame: 1 year ]
- Parts C1, C2, C3: Progression Free Survival (PFS) [ Time Frame: 1 year ]
- Parts C1, C2, C3: Response Duration (RD) [ Time Frame: 1 year ]
- Parts C1, C2, C3: Overall Survival (OS) [ Time Frame: 1 year ]
- Parts C1, C2, C3: Clinical benefit (Complete Response (CR) + Partial Response (PR) + Stable Disease (SD) of 6 months or greater) [ Time Frame: 1 year ]
- Parts C1, C2, C3: PK parameter estimates of M6620 including maximum concentrations (Cmax), area under the curve (AUC), apparent volume at steady state (Vss), clearance (CL) and terminal elimination half-life (t1/2) [ Time Frame: 1 year ]
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
Disease status
- Parts A and B/B2: Histologically or cytologically confirmed advanced solid tumor that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective, or for whom regimens containing gemcitabine, cisplatin, etoposide, and/or irinotecan might be considered, and with measurable disease according to RECIST criteria
- Part C1:
For Pre-screening:
- Advanced (metastatic or locally-advanced unresectable and not eligible for definitive treatment, e.g., surgery/radiotherapy), histologically confirmed non-small cell lung cancer (NSCLC)
- Available historical tumor specimen at the time of pre-screening or willing to provide a tumor biopsy (core) if the biopsy may be considered as part of standard clinical practice for the participant
- Received or did not tolerate standard approved targeted therapy, if appropriate for tumor genotype
For Screening:
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Measurable disease according to RECIST criteria
-Part C2:
- Advanced (locally-advanced incurable or metastatic) histologically confirmed estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2) negative breast cancer.
- Adequate available historical tumor specimen or willing to provide a tumor biopsy (core) if the biopsy may be considered as part of standard clinical practice for the participant
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Measurable disease according to RECIST criteria
-Part C3:
- Advanced (locally-advanced incurable or metastatic) histologically confirmed SCLC that is platinum-resistant, defined as disease progression during initial treatment with a platinum-based regimen or progression within 90 days of completion of platinum therapy. Participants with platinum-resistant disease may receive a second-line non-platinum-based chemotherapy and subsequently be enrolled to this study. Participants who received and are resistant to a second-line platinum-based chemotherapy may also be enrolled into the study.
- Adequate available historical tumor specimen or willing to provide a tumor biopsy (core) if the biopsy may be considered as part of standard clinical practice for the participant
- Measurable disease according to RECIST criteria
- WHO performance status of 0 or 1
- Life expectancy of >=12 week
- Hematological and biochemical indices within protocol specified ranges at screening.
Exclusion Criteria:
- Radiotherapy (except for palliative reasons) endocrine therapy, immunotherapy, or chemotherapy during the previous 4 weeks (6 weeks for nitrosoureas and Mitomycin-C, and 4 weeks for investigational medicinal products) or less than 4 drug half-lives, whichever greater, before first dose of study drug.
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Parts A, B and B2:
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Greater than 6 cycles of prior treatment with cisplatin and/or carboplatin.
- Part A/B: History of prior dose reductions or dose interruptions while receiving cisplatin or carboplatin due to toxicity from the platinum or intolerance to either agent.
- Part B2: Prior exposure to irinotecan is permitted except for participants with a known hypersensitivity reaction to irinotecan.
- Participants with a known history of Grade 4 thrombocytopenia or Grade 4 neutropenia while receiving prior therapy.
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Part C1:
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Any cytotoxic chemotherapy beyond 1 line of platinum-based chemotherapy. One additional line of non-platinum based therapy in the advanced setting
- Pre-screening Only*: Participants may currently be receiving platinum-based chemotherapy in the advanced setting, or have completed 1 line of platinum-based chemotherapy and are currently receiving a second-line non-platinum-based therapy or maintenance therapy
- There is no restriction on prior immunotherapy or targeted therapy unless combined together with a cytotoxic agent
- Any prior gemcitabine for the treatment of NSCLC in any setting within 6 months
- Participants who are known to be TP53 wild-type, unless they are determined to have ATM loss of expression during screening or pre-screening or until all the planned participants with TP53 mutation are enrolled as determined by the medical monitor
- Participants with unknown TP53 mutational status will be enrolled until the group of approximately 10 participants without TP53 mutation or until all the planned participants with TP53 mutation are enrolled as determined by the medical monitor
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Part C2:
- Any prior platinum therapy in the adjuvant or neoadjuvant within 6 months of screening
- Relapse within 3 months of completion of prior adjuvant or neoadjuvant chemotherapy
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Any prior chemotherapy in the metastatic setting with the exception of either a taxane or an anthracycline in the first-line metastatic setting
(a) There is no restriction on prior immunotherapy or targeted therapy in the metastatic setting unless combined together with a cytotoxic agent
- Participants with known BRCA1/BRCA2 germline mutations, either determined and documented prior to Screening, or determined during Screening. Participants with unknown BRCA1/BRCA2 status may be enrolled at discretion of the sponsor
- Participants who are documented to be non-basaloid subtype using molecular profiling assay (e.g. PAM50 assay) prior to Screening
- Participants with unknown BRCA1/BRCA2 or basaloid subtype status will be enrolled until the number of enrolled participant is approximately 40. If approximately 40 participants have been enrolled and a minimum of 30 participants who are basaloid positive and BRCA1/BRCA2 germline wild-type have not been enrolled, the basaloid subtype and BRCA status assay will be required at Screening to exclude participants who are basaloid negative or have BRCA1/BRCA2 germline mutations.
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Part C3:
- Prior platinum-sensitive participants , unless they progress on or within 90 days of completion of platinum-based regimen
- There is no restriction on prior immunotherapy or targeted therapy in the metastatic setting unless combined together with a cytotoxic agent
- During prior carboplatin therapy, requirement for dose reduction below AUC 5 mg.min/mL or discontinuation of carboplatin for toxicity or lack of tolerability.
- Unresolved toxicity of Common Terminology Criteria for Adverse Events (CTCAE) Grade 2 or greater from previous anti-cancer therapy or radiotherapy
- History of spinal cord compression or brain metastases, unless asymptomatic, treated, stable, and not requiring treatment with steroids for at least 4 weeks before first dose of study drug. Any history of leptomeningeal metastases.
- Female participants who are already pregnant or lactating, or plan to become pregnant within 6 months of the last dose of study drug are excluded. Female participants of childbearing potential must adhere to contraception guidelines
- Male participants with partners of child-bearing potential must agree to adhere to contraception guidelines. Men with pregnant or lactating partners or partners who plan to become pregnant during the study or within 6 months of the last dose of study drug are excluded
- Serious cardiac or other co-morbid disease, as specified in the protocol
- Prior bone marrow transplant or extensive radiotherapy to greater than 15% of bone marrow
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Part C:
- Current malignancies of other types, with the exception of adequately treated cone-biopsied in situ carcinoma of the cervix uteri and basal or squamous cell carcinoma of the skin
- Major surgery =<2 weeks before starting study drug, or incomplete recovery from a prior major surgical procedure.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02157792
Locations
Show 31 study locations
Sponsors and Collaborators
EMD Serono Research & Development Institute, Inc.
Merck KGaA, Darmstadt, Germany
Investigators
| Study Director: | Medical Responsible | EMD Serono Research & Development Institute, Inc., a subsidiary of Merck KGaA, Darmstadt, Germany |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | EMD Serono Research & Development Institute, Inc. |
| ClinicalTrials.gov Identifier: | NCT02157792 |
| Other Study ID Numbers: |
MS201923_0001 VX12-970-001 ( Other Identifier: Other ) 2012-003126-25 ( EudraCT Number ) |
| First Posted: | June 6, 2014 Key Record Dates |
| Last Update Posted: | April 1, 2020 |
| Last Verified: | March 2020 |
Keywords provided by EMD Serono ( EMD Serono Research & Development Institute, Inc. ):
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Solid Tumor Advanced Solid Tumor VX12-970-001 M6620 VX-970 |
Gemcitabine Cisplatin Etoposide Carboplatin Irinotecan |
Additional relevant MeSH terms:
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Neoplasms Carboplatin Gemcitabine Irinotecan Etoposide Antineoplastic Agents Antimetabolites, Antineoplastic |
Antimetabolites Molecular Mechanisms of Pharmacological Action Topoisomerase I Inhibitors Topoisomerase Inhibitors Enzyme Inhibitors Antineoplastic Agents, Phytogenic Topoisomerase II Inhibitors |