Autogene Cevumeran + Pembrolizumab for Melanoma

(IMCODE001 Trial)

No longer recruiting at 80 trial locations
RS
RS
Overseen ByReference Study ID Number: IMCODE001(GO40558) https://forpatients.roche.com/
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Genentech, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment combination for people with advanced melanoma. It aims to evaluate the effectiveness of autogene cevumeran (an experimental treatment) when combined with pembrolizumab, compared to pembrolizumab alone. Participants will be divided into groups to receive either pembrolizumab alone or with autogene cevumeran. This trial suits those with advanced melanoma who have not received previous systemic treatment and do not have eye-related melanoma or significant liver disease. As a Phase 2 trial, the research focuses on assessing the treatment's effectiveness in an initial, smaller group of people.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research shows that pembrolizumab, one of the treatments in this trial, is generally well-tolerated. The FDA has already approved it for treating melanoma and other conditions. Common side effects may include tiredness, skin rash, and mild nausea. Although less common, more serious side effects can occur and may involve the immune system.

Less information is available about autogene cevumeran. This treatment is still under study, so detailed safety data remains limited. However, since this is a Phase 2 trial, earlier studies have shown it is safe enough for further research. Participants might experience some side effects, but the details are still under investigation.

Overall, researchers are carefully studying the combination of autogene cevumeran and pembrolizumab to understand its tolerability and monitor any side effects.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about Autogene Cevumeran combined with Pembrolizumab for melanoma because it represents a novel approach to treatment. Most current therapies for melanoma rely on targeting specific pathways to inhibit cancer growth, like BRAF and MEK inhibitors or immune checkpoint inhibitors such as Pembrolizumab alone. However, Autogene Cevumeran is a personalized cancer vaccine that works by stimulating the immune system to recognize and attack melanoma cells more effectively. This combination aims to enhance the immune response beyond what Pembrolizumab can achieve on its own, offering hope for improved outcomes in melanoma treatment.

What evidence suggests that this trial's treatments could be effective for advanced melanoma?

This trial will compare the effectiveness of pembrolizumab alone with the combination of autogene cevumeran and pembrolizumab for treating advanced melanoma. Research has shown that adding autogene cevumeran to pembrolizumab does not improve results compared to using pembrolizumab alone. Pembrolizumab is a well-known and effective treatment for melanoma. Although autogene cevumeran is an experimental treatment designed to work with pembrolizumab, the evidence so far does not show any added benefit from combining the two. Thus, the combination currently does not seem to offer more than pembrolizumab by itself.13456

Who Is on the Research Team?

CT

Clinical Trials

Principal Investigator

Hoffmann-La Roche

Are You a Good Fit for This Trial?

This trial is for adults with advanced melanoma that hasn't been treated before. They should have a certain level of physical fitness (ECOG 0 or 1), a life expectancy of at least 12 weeks, and their major organs must be functioning well. People can't join if they've had organ transplants, significant heart disease, liver problems, eye melanoma, untreated brain metastases, autoimmune diseases, HIV/AIDS, hepatitis B or C.

Inclusion Criteria

Your disease can be measured using a specific method called RECIST v1.1.
I have advanced melanoma and haven't received systemic anti-cancer treatments, with some exceptions.
My blood and organs are functioning well.
See 4 more

Exclusion Criteria

I have had my spleen removed.
I have active hepatitis B, C, or tuberculosis.
I have not had any cancer treatment except those allowed in the study.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Safety Run-in

Participants receive at least one cycle of 200 mg pembrolizumab monotherapy by IV infusion followed by 200 mg pembrolizumab IV infusion every 3 weeks plus a recommended dose of autogene cevumeran

6 weeks
2 visits (in-person)

Randomized Treatment

Participants receive either pembrolizumab alone or in combination with autogene cevumeran, with the option to cross over to combination treatment after confirmed disease progression

24 months
8 visits (in-person) every 3 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Pembrolizumab
  • RO7198457
Trial Overview The study is testing the combination of Autogene cevumeran (RO7198457) with Pembrolizumab versus using Pembrolizumab alone in patients who haven't received treatment for their advanced melanoma. It aims to see which approach works better and how safe it is.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Active Control
Group I: Safety Run-in Period: Autogene Cevumeran + PembrolizumabExperimental Treatment2 Interventions
Group II: Randomized Period: Arm B: Autogene Cevumeran + PembrolizumabExperimental Treatment2 Interventions
Group III: Randomized Period: Arm A: PembrolizumabActive Control1 Intervention

Pembrolizumab is already approved in United States, European Union, United Kingdom for the following indications:

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Approved in United States as KEYTRUDA for:
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Approved in European Union as KEYTRUDA for:
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Approved in United Kingdom as KEYTRUDA for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Genentech, Inc.

Lead Sponsor

Trials
1,578
Recruited
569,000+
Ashley Magargee profile image

Ashley Magargee

Genentech, Inc.

Chief Executive Officer since 2024

MBA from Harvard University, BA from Princeton University

Levi Garraway profile image

Levi Garraway

Genentech, Inc.

Chief Medical Officer since 2021

MD, PhD

BioNTech SE

Industry Sponsor

Trials
84
Recruited
120,000+

Prof. Dr. Ugur Sahin

BioNTech SE

Chief Executive Officer since 2008

MD from University of Cologne

Prof. Özlem Türeci

BioNTech SE

Chief Medical Officer since 2018

MD from Saarland University

Citations

LPS GO40558 Final Results July 2025 English - ForPatientsUnfortunately, the study found that adding autogene cevumeran to pembrolizumab did not improve results compared to using pembrolizumab alone in ...
2.clinicaltrials.biontech.comclinicaltrials.biontech.com/trials/GO40558
A Study to Evaluate the Efficacy and Safety of Autogene ...This study will evaluate the efficacy, safety, pharmacokinetics, and patient-reported outcomes (PROs) of autogene cevumeran (RO7198457) plus pembrolizumab ...
Clinical trial for Skin Cancer, Advanced Melanoma-Genente...This study will evaluate the efficacy, safety, pharmacokinetics, and patient-reported outcomes (PROs) of autogene cevumeran (RO7198457) plus pembrolizumab
Study on the Effectiveness and Safety of RO7198457 ...This study examines the safety and effectiveness of RO7198457 (Autogene Cevumeran) and Pembrolizumab (Keytruda) in treating patients with ...
A Study to Evaluate the Efficacy and Safety of Autogene ...This study will evaluate the efficacy, safety, pharmacokinetics, and patient-reported outcomes (PROs) of autogene cevumeran (RO7198457) plus pembrolizumab ...
Record History | ver. 5: 2019-06-03 | NCT03815058A Study to Evaluate The Efficacy And Safety Of RO7198457 In Combination With Pembrolizumab Versus Pembrolizumab Alone In Participants With Previously Untreated ...
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