A Phase 2, Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled Clinical Study of V940 (mRNA-4157) Plus Pembrolizumab Versus Placebo Plus Pembrolizumab in Participants With First-Line Advanced Melanoma (INTerpath-012)

Status: Recruiting
Location: See all (28) locations...
Intervention Type: Other, Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Researchers want to learn if V940 with pembrolizumab can stop advanced melanoma from growing or spreading. Melanoma is a type of skin cancer. Advanced means the cancer has spread to other parts of the body and cannot be removed with surgery. A standard (or usual) treatment for advanced melanoma is immunotherapy. Immunotherapy is a treatment that helps the immune system fight cancer. V940 is a study treatment designed to help a person's immune system attack their specific cancer. Pembrolizumab is an immunotherapy. The goal of this study is to learn if people who receive V940 with pembrolizumab live longer without the cancer growing or spreading than people who receive placebo with pembrolizumab. A placebo looks like the study treatment but has no study treatment in it. Using a placebo helps researchers better understand the effects of a study treatment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ The main inclusion criteria include but are not limited to the following:

• Has unresectable and histologically confirmed Stage III or IV cutaneous melanoma per American Joint Committee on Cancer (AJCC) Eighth Edition guidelines.

• Has been untreated for melanoma except if participant received prior adjuvant or neoadjuvant therapy with targeted therapy or immunotherapy (such as anti-cytotoxic T-lymphocyte-associated protein \[CTLA-4\], anti-programmed cell death 1 protein \[PD-1\] therapy or interferon), and only if relapse did not occur within 12 months after treatment discontinuation.

• Have documentation of serine/threonine-protein kinase B-raf (BRAF) V600-activating mutation status or had BRAF V600 mutation testing per local institutional standards during the screening period (participants with BRAF mutation positive melanoma as well as BRAF wild-type or unknown are eligible).

• Have the presence of at least 1 measurable lesion by computed tomography (CT) or magnetic resonance imaging (MRI) per Response Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as determined by the local site investigator/radiology assessment.

• Provides tumor tissue (preferably from a metastatic site and, if not available, from the primary tumor) that is suitable for next generation sequencing and biomarker analysis as required for this study.

• Participants with human immunodeficiency virus (HIV) must have well controlled HIV on antiretroviral therapy (ART).

• Participants who are hepatitis B surface antigen (HBsAg) positive are eligible if they have received hepatitis B virus (HBV) antiviral therapy for at least 4 weeks, and have undetectable HBV viral load prior to randomization.

• Participants with history of hepatitis C virus (HCV) infection are eligible if HCV viral load is undetectable at screening.

Locations
United States
Arkansas
Highlands Oncology Group ( Site 4042)
RECRUITING
Springdale
California
UCSF Helen Diller Medical Center at Parnassus Heights ( Site 4044)
RECRUITING
San Francisco
New Jersey
John Theurer Cancer Center at Hackensack University Medical Center ( Site 4047)
RECRUITING
Hackensack
Washington
Fred Hutchinson Cancer Center ( Site 4041)
RECRUITING
Seattle
Other Locations
Australia
Blacktown Hospital ( Site 2001)
RECRUITING
Blacktown
One Clinical Research ( Site 2002)
RECRUITING
Nedlands
Melanoma Institute Australia ( Site 2000)
RECRUITING
Wollstonecraft
France
Centre Hospitalier Universitaire de Nice - Hôpital l'Archet-Dermatology Department ( Site 2042)
RECRUITING
Nice
Hôpital Saint-Louis ( Site 2041)
RECRUITING
Paris
Gustave Roussy ( Site 2040)
RECRUITING
Villejuif
Germany
Universitaetsklinikum Koeln ( Site 2064)
RECRUITING
Cologne
Universitaetsklinikum Hamburg-Eppendorf ( Site 2060)
RECRUITING
Hamburg
NCT ( Site 2065)
RECRUITING
Heidelberg
Greece
Metropolitan Hospital ( Site 2082)
RECRUITING
Athens
European Interbalkan Medical Center ( Site 2081)
RECRUITING
Thessaloniki
Israel
Emek Medical Center ( Site 3003)
RECRUITING
Afula
Hadassah Medical Center ( Site 3001)
RECRUITING
Jerusalem
Rabin Medical Center ( Site 3002)
RECRUITING
Petah Tikva
Sheba Medical Center ( Site 3000)
RECRUITING
Ramat Gan
Italy
Istituto Nazionale Tumori IRCCS Fondazione Pascale ( Site 3020)
RECRUITING
Napoli
New Zealand
Harbour Cancer & Wellness ( Site 3040)
RECRUITING
Auckland
Poland
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie ( Site 3060)
RECRUITING
Warsaw
Portugal
Unidade Local de Saude de Santa Maria - Hospital de Santa Maria ( Site 4001)
RECRUITING
Lisbon
Unidade Local de Saude Lisboa Ocidental - Hospital de São Francisco Xavier ( Site 4002)
RECRUITING
Lisbon
Instituto Português de Oncologia do Porto Francisco Gentil, EPE ( Site 4000)
RECRUITING
Porto
Spain
Hospital Clínic Barcelona ( Site 3080)
RECRUITING
Barcelona
Hospital Universitari Vall d'Hebron ( Site 3081)
RECRUITING
Barcelona
Hospital Universitario Ramón y Cajal-Medical Oncology ( Site 3082)
RECRUITING
Madrid
Contact Information
Primary
Toll Free Number
Trialsites@msd.com
1-888-577-8839
Time Frame
Start Date: 2025-05-29
Estimated Completion Date: 2031-09-05
Participants
Target number of participants: 160
Treatments
Experimental: V940 + Pembrolizumab
Participants will receive 1 mg of V940 via intramuscular (IM) injection every 3 weeks (q3w) for up to 9 doses (up to approximately 27 weeks) plus 400 mg of pembrolizumab via intravenous (IV) infusion every 6 weeks (q6w) for up to 17 doses, or for a total treatment duration of up to approximately 2 years, or until disease progression or discontinuation.
Active_comparator: Placebo + Pembrolizumab
Participants will receive placebo via IM injection q3w for up to 9 doses (up to approximately 27 weeks) plus 400 mg of pembrolizumab via IV infusion q6w for up to 17 doses, or for a total treatment duration of up to approximately 2 years, or until disease progression or discontinuation.
Related Therapeutic Areas
Sponsors
Leads: Merck Sharp & Dohme LLC

This content was sourced from clinicaltrials.gov

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