Study Comparing Naporafenib and Trametinib Combination to Other Therapies for Patients with Previously Treated Unresectable or Metastatic NRAS Mutant Melanoma

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What is this study about?

This clinical trial is focused on studying treatments for unresectable or metastatic NRAS mutant cutaneous melanoma, a type of skin cancer that cannot be removed by surgery and has spread to other parts of the body. The study will explore the effectiveness of a combination of two medications: naporafenib and trametinib. Naporafenib, also known by its code name LXH254, is a medication that targets specific proteins involved in cancer cell growth. Trametinib is another medication that works by inhibiting certain proteins that help cancer cells grow and divide.

The purpose of the study is to compare the combination of naporafenib and trametinib with other treatments chosen by doctors, which may include dacarbazine, temozolomide, or trametinib alone. Dacarbazine and temozolomide are chemotherapy medications that work by damaging the DNA of cancer cells, preventing them from growing. The study will begin with a phase to determine the best dose of the naporafenib and trametinib combination. After this, the main part of the study will compare how well patients do on the combination treatment versus the other treatment options.

Participants in the study will receive their assigned treatment and be monitored over a period of time to assess the effects on their cancer. The study will look at how long patients live without their cancer getting worse and their overall survival. The trial will also monitor the safety of the treatments and any side effects that may occur. This research aims to find the most effective treatment option for patients with this specific type of melanoma.

1 joining the study

Upon joining the study, the patient will be informed about the trial’s purpose and procedures. Written consent is required to participate.

Eligibility criteria include being 18 years or older, having a confirmed diagnosis of unresectable or metastatic NRAS mutant cutaneous melanoma, and having previously received an anti-PD-1/L1 based treatment.

2 stage 1: dose optimization

The initial phase involves determining the optimal dose of the combination of naporafenib and trametinib.

Patients will receive these medications orally. The specific dosage will be adjusted based on safety and effectiveness data collected during this stage.

3 stage 2: treatment assignment

Patients will be randomly assigned to receive either the combination of naporafenib and trametinib or a treatment chosen by the physician, which could be dacarbazine, temozolomide, or trametinib alone.

The choice of therapy will depend on the patient’s specific condition and previous treatments.

4 medication administration

The combination of naporafenib and trametinib is administered orally. Dacarbazine is given intravenously, while temozolomide is taken orally.

The frequency and duration of administration will be determined by the study protocol and the patient’s response to treatment.

5 monitoring and assessments

Regular monitoring will occur to assess the treatment’s effectiveness and any side effects. This includes blood tests, imaging studies, and physical examinations.

Patients will be evaluated for progression-free survival and overall survival, as well as any adverse effects from the medications.

6 end of study participation

The study is expected to conclude by July 2028. Participation may end earlier if the patient experiences significant side effects or if the disease progresses.

Upon completion, patients will receive information about their treatment outcomes and any further steps if necessary.

Who Can Join the Study?

  • The patient must agree to participate by signing a written consent form.
  • The patient must be at least 18 years old.
  • The patient must have a type of skin cancer called unresectable or metastatic cutaneous melanoma, confirmed by a lab test.
  • The patient must have a specific change in their cancer called an NRAS mutation, confirmed by a test on tumor tissue or blood.
  • The patient must have a sample of their tumor collected within the last 5 years available for further analysis.
  • The patient must have previously received a treatment called anti-PD-1/L1 therapy and shown disease progression during or shortly after this treatment.
  • The patient must have an ECOG performance status of 0, 1, or 2, which is a scale that measures how well they can perform daily activities.
  • The patient must have at least one tumor that can be measured by doctors using a standard method called RECIST v1.1.
  • The patient must be able to swallow pills.

Who Cannot Join the Study?

  • Patients who have a type of skin cancer called NRAS mutant cutaneous melanoma that cannot be removed by surgery or has spread to other parts of the body.
  • Patients who are not within the specified age range for the study.
  • Patients who are not part of the specified clinical trial groups.
  • Patients who are not male or female, as both genders are included in the study.
  • Patients who are considered part of a vulnerable population, which means they might need special protection or care.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Ospedale San Raffaele S.r.l. Milan Italy
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Hospital General Universitario Gregorio Maranon Madrid Spain
Masarykuv Onkologicky Ustav Brno-Stred Czechia
Otto Von Guericke Universitaet Magdeburg Magdeburg Germany
Centre Hospitalier Le Mans Le Mans France
University Hospital Olomouc Olomouc Czechia
Complejo Hospitalario Universitario Insular Materno Infantil Las Palmas De Gran Canaria Spain
Radboud universitair medisch centrum Nijmegen The Netherlands
Heidelberg University Mannheim Germany
Assistance Publique Hopitaux De Paris Boulogne-Billancourt France
Cexubstpw Uwwqtsjvszlnhs Szdgedszi Woluwe-Saint-Lambert Belgium
Hgvtbubs Vlvl doguscqx Barcelona Spain
Cpbndu Hxxpaarfhpl Ujjjnyglnrcri Dl Cyza Nnuvhqhur Caen France
Hniilj Hfkqkldh Herlev Denmark
Uwuwttxohtncyliwvvxiw Edjfidku Asl Erlangen Germany
Ueiljvyotpszvlknfsncg Teouuslcu Agk Tuebingen Germany
Arhslckxt Uxp Amsterdam The Netherlands
Asolouzgwu Pzqwbuah Hteyvafx Dx Mlwntzoba Marseille France
Akxpwpiw Uzardbkpmm Hwzcjxmw Lorenskog Norway
Hkezvuij Cpvsfv Dd Bzstqwrmd Barcelona Spain
Cknmvjv Unfbbctcogytgpxosumt Buejia Kje Berlin Germany
Epykzfd Ubkwounrefxs Mwlqrdn Cyvjuqy Ryfepyxse (vvsdztx Mbp Rotterdam The Netherlands
Abwmizw Uxxnbpthio Hvvvpopn Aalborg Denmark
Mjytmjs Clnwoa &xwildh Uwkawugwis Oa Fylswbne Freiburg Im Breisgau Germany
Kcftanuf dvm Ummquryfzrgf Mixvnyhi Avv Munich Germany
Ujkllkyycwzp Lvibmma Leipzig Germany
Iabodo Ilnegzry Ffsynxgtqehuf Ojczgkjctkn Rome Italy
Rcmkbm Olanqyp Lmay Orebro Sweden
Uxnaxizexwbt Ztrzksjcba Gnvl Gent Belgium
Uuygxyimmhahbvogtihzp Skpnnalapvuzxpedpm Axb Kiel Germany
Aveoudi Sqslovxer Umzzfcnhowiya Fzrjhz Cexbechx Udine Italy
Crnkzo Hkmxvhthfnw Lbvd Ssy Pierre Benite France
Viuby Uyhvdknqnqqg Blajzjt Jette Belgium
Htbnw Sekimdhej Hy Stavanger Norway
Ipacwvxq Czrybq Dwdmuphzwdpyblesv L'hospitalet De Llobregat Spain
Iskedvmr Tsizcc Bmjb Gpjmmvup Pwvhj Iv Bari Italy
Fxhvazedg Ivkwrobhq Vmksykwfdy Dy Onbeedteu Valencia Spain
Fpkesscrcl Iobdl Sqr Gxituna Dmg Tzrgarj Monza Italy
Fhbnophqlb Iramebysdz Ikvctase Nwyhhkgdlbe Bmzbs Milan Italy
Iiqesctt Ozujdahyra Vylqct Padua Italy
Colyqb Du Ljebb Cmckyy Lg Cfmcnr Esfzcq Mhlcjdm Rennes France
Csaais Hxznhecbqoz Ucwxfsnipyeks Da Djasq Dijon France
Avjuziyvcs Plxrdkeu Hvhttblr Df Papux Paris France
Aumthjg Ordutyrditt Uahodyqoesawd Sxatoq Siena Italy
Axjbwj Uxzuyadnkh Hkizlevn Aarhus Denmark
Lfhwe Uvuqizkzymro Mcugovy Clrhgac (lgjgf Leiden The Netherlands
Fzdmwlsfcl Lktnj Mucto Mkudf Rome Italy
Ixumz Kpvhgmrju Solbwsdok Zwolle The Netherlands
Hbrglriz Stufr Mcjuq Dkfdu Mntzeflrelbt Perugia Italy
Mhhtsuccnbyjxdzvabfx Ard Minden Germany
Gojlqskfbm Nxxa gwbsv Kdykoqtrpczim Bkgeji Bremen Germany
Fhaickvwhx Htciscixm evbd Munster Germany
Absjikzoxt Zsbbmwikia Mgaydiqkkr Maastricht The Netherlands
Czgqoh Huvplfemzps Uuauvcshriwqq De Bgruunfu Bordeaux France
Clijan Hidbkckdrjl Ubdrzidqjrtvp Da Ndzm Nice France
Myljpac Csakdlt Lvguuhznff Bbsb Leeuwarden The Netherlands
Vjlixutpa Fyhameji Nxkddutdz V Pvvwl Prague Czechia
Kobyoohcnn Umaiiqjpnn Hqqcyehs Stockholm Sweden

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
27.09.2024
Czechia Czechia
Not recruiting
27.09.2024
Denmark Denmark
Not recruiting
27.09.2024
France France
Not recruiting
27.09.2024
Germany Germany
Not recruiting
27.09.2024
Italy Italy
Not recruiting
27.09.2024
Norway Norway
Not recruiting
27.09.2024
Spain Spain
Not recruiting
27.09.2024
Sweden Sweden
Not recruiting
27.09.2024
The Netherlands The Netherlands
Not recruiting
27.09.2024

Trial locations

Naporafenib is an investigational medication being studied for its potential to treat patients with a specific type of skin cancer known as NRAS mutant cutaneous melanoma. It is being tested in combination with another medication to see if it can help improve outcomes for patients whose cancer cannot be surgically removed or has spread to other parts of the body.

Trametinib is a medication used to treat certain types of skin cancer. In this trial, it is being used both in combination with naporafenib and as a standalone treatment option. The study aims to determine the effectiveness of trametinib when used alone or in combination with naporafenib.

Dacarbazine is a chemotherapy drug that is used to treat melanoma. In this trial, it is one of the treatment options that doctors can choose for patients. The study is comparing the effectiveness of dacarbazine to other treatments to see which works best for patients with this type of skin cancer.

Temozolomide is another chemotherapy medication that is used to treat melanoma. It is included in the trial as one of the treatment options available to doctors. The trial is evaluating how well temozolomide works compared to other treatments for patients with NRAS mutant cutaneous melanoma.

Unresectable or Metastatic NRAS Mutant Cutaneous Melanoma – This is a type of skin cancer that occurs when melanocytes, the cells responsible for skin pigment, grow uncontrollably. It is characterized by a mutation in the NRAS gene, which can lead to aggressive tumor growth. The term “unresectable” indicates that the cancer cannot be removed completely through surgery. When the disease is metastatic, it means that the cancer has spread from its original site to other parts of the body. The progression of this melanoma can vary, but it often involves the development of new tumors in distant organs. The condition is typically monitored through imaging and clinical evaluations to assess the spread and growth of the cancer.

Trial ID:
2024-511404-17-00
Protocol code:
ERAS-254-02
NCT ID:
NCT06346067
Trial Phase:
Therapeutic confirmatory (Phase III)

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