Study of IO102-IO103 and Pembrolizumab for Patients with Advanced Melanoma

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What is this study about?

This clinical trial is focused on studying a type of skin cancer called melanoma, specifically in cases where the cancer is advanced and cannot be removed by surgery. The study is investigating the effectiveness of a new treatment combination. The treatment involves two medications: IO102-IO103 and pembrolizumab. Pembrolizumab is already used in treating melanoma, while IO102-IO103 is being tested to see if it can improve outcomes when used together with pembrolizumab.

The purpose of the study is to compare the combination of IO102-IO103 and pembrolizumab against pembrolizumab alone. Participants in the study will receive either the combination treatment or pembrolizumab by itself. The study will monitor how long patients live without the cancer getting worse, which is known as progression-free survival. The trial will also look at other outcomes, such as the overall response rate, which measures how many patients experience a reduction in cancer size, and overall survival, which tracks how long patients live after starting the treatment.

Participants will be randomly assigned to one of the two treatment groups and will receive their treatment through injections. The study will continue for a period of up to 24 months, during which time patients will be regularly monitored to assess the effectiveness and safety of the treatments. This trial aims to provide valuable information on whether the new combination treatment can offer better results for patients with advanced melanoma.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria, including a diagnosis of advanced melanoma and no prior systemic treatment for this condition.

A biopsy and blood samples are collected for biomarker assessments.

2 randomization

Participants are randomly assigned to one of two groups: one receiving pembrolizumab alone, and the other receiving a combination of IO102-IO103 and pembrolizumab.

3 treatment administration

For those receiving pembrolizumab alone, the medication is administered as an intravenous infusion.

For those receiving the combination treatment, pembrolizumab is administered intravenously, and IO102-IO103 is given as a subcutaneous injection.

The specific dosage and frequency of administration are determined by the study protocol.

4 monitoring and assessments

Regular monitoring is conducted to assess the response to treatment and any side effects.

Progression-free survival (PFS) is evaluated, which measures the time until the disease progresses or the patient passes away.

5 end of treatment

The treatment continues until disease progression, unacceptable side effects, or other criteria specified in the study protocol are met.

Final assessments are conducted to evaluate the overall response rate and overall survival.

Who Can Join the Study?

  • The patient must have a type of skin cancer called melanoma that is either not treatable with surgery or has spread to other parts of the body.
  • The patient should not have received any previous treatment for this type of cancer, except in certain cases where previous treatments were given more than 6 months ago and did not result in a relapse during or shortly after treatment.
  • The patient must have a performance status score of 0 or 1, which means they are fully active or have some symptoms but can still carry out light work.
  • The patient should have a life expectancy of more than 24 weeks, as assessed by the doctor.
  • The patient must have at least one tumor that can be measured to see how the cancer responds to treatment.
  • The patient needs to provide a sample of their tumor tissue and blood for testing. This can be a recent sample or a new one taken during the screening process.
  • Both men and women can participate in the study.
  • The study includes adults and older adults.

Who Cannot Join the Study?

  • Patients who have already received treatment for their melanoma.
  • Patients whose melanoma can be surgically removed.
  • Patients who do not have melanoma that has spread to other parts of the body (metastatic melanoma).
  • Patients who are not within the specified age range for the study.
  • Patients who are not able to give informed consent or are part of a vulnerable population.
  • Patients who have other medical conditions that might interfere with the study.
  • Patients who are pregnant or breastfeeding.
  • Patients who are participating in another clinical trial.
  • Patients who have allergies to the study medications.
  • Patients who have had a recent major surgery.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Istituto Oncologico Veneto Padua Italy
Orszagos Onkologiai Intezet Budapest Hungary
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Fondazione Luigi Maria Monti Rome Italy
Universitair Ziekenhuis Gent Gent Belgium
St. Josef-Hospital Bochum Germany
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Santa Maria Della Misericordia Perugia Italy
Istituto Tumori Bari Giovanni Paolo II Bari Italy
Muehlenkreiskliniken AöR Minden Germany
Vitaz Sint-Niklaas Belgium
Jasz-Nagykun-Szolnok Varmegyei Hetenyi Geza Korhaz-Rendelointezet Szolnok Hungary
Elbe Kliniken Stade-Buxtehude gGmbH Buxtehude Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Odense University Hospital Odense Denmark
Universitaetsklinikum Erlangen AöR Erlangen Germany
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Hospital Clinic De Barcelona Barcelona Spain
Charite Universitaetsmedizin Berlin KöR Berlin Germany
SLK-Kliniken Heilbronn GmbH Heilbronn Germany
Hopital Ambroise Pare Boulogne-Billancourt France
Fakultni Nemocnice Kralovske Vinohrady Prague Czechia
IRCCS Ospedale Policlinico San Martino Genoa Italy
Hospital General Universitario De Valencia Valencia Spain
Aalborg University Hospital Aalborg Denmark
Centre Hospitalier Universitaire De Nice Nice France
Region Midtjylland Aarhus Denmark
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
University Hospital Olomouc Olomouc Czechia
University Of Pecs Pecs Hungary
Netherlands Cancer Institute Amsterdam The Netherlands
Centre Hospitalier Lyon Sud Pierre Benite France
Institut de Cancérologie de l’Ouest Saint-Herblain France
University Hospital Ostrava Ostrava Czechia
Centre De Lutte Contre Le Cancer Eugene Marquis Rennes France
Uyzwzqtjtjqttdmxbdgfl Etesv Anh Essen Germany
Iekgfd Ifxqipra Fgdpeemffbeuk Oxakkgvikop Rome Italy
Laatb Usilfirbxcxe Mwwnogr Czvpzhc (jwsad Leiden The Netherlands
Ulosdipuaxgiltibdyjox Aximmkgn Augsburg Germany
Cvhgna Hjojozwqflx Vwqithz Valence France
Iwoxvkxso Oltdskvpeu Dlt Rswqak Sxrg Barcelona Spain
Hxndew Hjvwjfyn Herlev Denmark
Ildaxqwx Rogvweayn Pko Lz Sjzsmw Dve Tgkxqp Dcyv Alefsql Iaji Sbdcgn Meldola Italy
Akzlxldlo Uxj Amsterdam The Netherlands
Aikrmystjo Pzyvrxkk Havwqgbi Dl Mhlkggdew Marseille France
Brfgmkbf Uypsimiqgo Hxxoulen Clfytk Besançon France
Eaqfxqo Usrazyxapgpc Motpbmg Chdejlo Rymqekzgm (xrjlaqy Mxy Rotterdam The Netherlands
Ahndcjs Oeqfcjboprz Ucwqfkszzbvfw Srlzmt Siena Italy
Uokpbkhdsivnusrlvritl Mrctrdus Ats Munster Germany
Ndadjvzp Iofqzbed Oniquqgaz Icp Mvcxz Sjnedwophlmyelekdrdqjovrjwou Irihxdnp Boxwqrjf Cracow Poland
Kceblwos dyw Uensxrpsykmg Mhvubhph Atx Munich Germany
Uzpefkgkkizjfzaysbrep Wnykeicds Aez Wuerzburg Germany
Ijecvhga Ccjgpy Dihztrvprmepfwrrj L'hospitalet De Llobregat Spain
Hywkxlbc Vojv deuvpzcr Barcelona Spain
Hmgyrcjx Utkepiktuqofv dm A Cnpfie A Coruna Galicia Spain

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
30.12.2020
Czechia Czechia
Not recruiting
30.12.2020
Denmark Denmark
Not recruiting
30.12.2020
France France
Not recruiting
30.12.2020
Germany Germany
Not recruiting
30.12.2020
Hungary Hungary
Not recruiting
30.12.2020
Italy Italy
Not recruiting
30.12.2020
Poland Poland
Not recruiting
30.12.2020
Spain Spain
Not recruiting
30.12.2020
The Netherlands The Netherlands
Not recruiting
30.12.2020

Trial locations

Investigated drugs:

IO102-IO103 is an investigational therapy being studied for its potential to treat advanced melanoma. It is used in combination with another medication to see if it can improve outcomes for patients with this type of skin cancer. The goal is to determine if this combination can help patients live longer without their disease getting worse.

Pembrolizumab is a medication that helps the immune system fight cancer cells. It is already used to treat various types of cancer, including melanoma. In this trial, it is being used both alone and in combination with IO102-IO103 to see if the combination offers any additional benefits for patients with advanced melanoma.

Investigated diseases:

Melanoma – Melanoma is a type of skin cancer that develops from the pigment-producing cells known as melanocytes. It is characterized by the uncontrolled growth of these cells, often appearing as a new or changing mole on the skin. Melanoma can occur on any skin surface, but it is more common in areas exposed to the sun. If not detected early, melanoma can spread to other parts of the body, including lymph nodes and internal organs. The progression of melanoma is typically categorized by stages, which describe the extent of the disease’s spread. Early detection and monitoring of skin changes are crucial in managing the progression of melanoma.

Trial ID:
2024-511996-13-00
Protocol code:
IOB-013/KN-D18
NCT ID:
NCT05155254
Trial Phase:
Therapeutic confirmatory (Phase III)

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