Study of INBRX-106 and Pembrolizumab for First-Line Treatment in Patients with Recurrent or Metastatic Head and Neck Cancer

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What is this study about?

This clinical trial is focused on studying a type of cancer called Head and Neck Squamous Cell Carcinoma (HNSCC), which can occur in areas such as the mouth, throat, and voice box. The study is looking at patients whose cancer has come back or spread to other parts of the body and who have a specific protein called PD-L1 present in their tumors. The trial will test the effectiveness of a new treatment combination using two medications: INBRX-106 and Pembrolizumab, also known by its brand name KEYTRUDA. Pembrolizumab is a type of medicine called a monoclonal antibody, which helps the immune system fight cancer. INBRX-106 is another type of antibody that targets a specific part of the immune system to help it work better against cancer.

The purpose of the study is to compare the effectiveness of the combination of INBRX-106 and Pembrolizumab against Pembrolizumab alone. Some patients will receive the combination treatment, while others will receive only Pembrolizumab. A third group will receive a placebo, which looks like the treatment but does not contain any active medicine. The study will help determine if adding INBRX-106 to Pembrolizumab provides better outcomes for patients with this type of cancer.

Participants in the study will receive their assigned treatment through an intravenous infusion, which means the medicine is given directly into a vein. The study will last for a period of up to 105 weeks, during which time patients will be monitored regularly to assess how well the treatment is working and to check for any side effects. The goal is to find out if the new combination treatment can improve the chances of controlling the cancer and extending the lives of patients with recurrent or metastatic HNSCC.

1 initial treatment phase

The study involves two main treatments: INBRX-106 and pembrolizumab. Pembrolizumab is administered as a 25 mg/mL concentrate for solution for infusion. INBRX-106 is given as a solution for injection.

Both medications are administered intravenously, meaning they are given directly into a vein. The specific dosage and frequency will be determined by the study protocol and the healthcare team.

2 treatment administration

The treatment is given in cycles. Each cycle’s duration and the number of cycles will be specified by the healthcare team based on the study protocol.

During each cycle, the patient will receive the assigned treatment, which may include either pembrolizumab alone or a combination of INBRX-106 and pembrolizumab.

3 monitoring and assessments

Regular monitoring will occur to assess the patient’s response to the treatment. This includes physical examinations, blood tests, and imaging studies as needed.

The healthcare team will evaluate the effectiveness of the treatment and monitor for any side effects or adverse reactions.

4 follow-up and evaluation

After completing the treatment cycles, follow-up visits will be scheduled to continue monitoring the patient’s health and response to the treatment.

The study aims to compare the effectiveness of the combination treatment versus pembrolizumab alone in terms of overall response rate, progression-free survival, and overall survival.

Who Can Join the Study?

  • Able to understand and provide written informed consent.
  • Life expectancy of more than 3 months.
  • Adequate organ function based on screening lab tests done within 3 days of starting the study. This includes:
    • Hematological (blood-related) function:
      • Enough neutrophils (a type of white blood cell) without needing a transfusion or growth factor support.
      • Enough platelets (cells that help with blood clotting).
      • Enough hemoglobin (a protein in red blood cells that carries oxygen).
    • Renal (kidney-related) function:
      • Normal creatinine levels (a waste product filtered by the kidneys) or a creatinine clearance rate that meets the study’s standards.
    • Hepatic (liver-related) function:
      • Enough albumin (a protein made by the liver).
      • Normal levels of AST and ALT (enzymes that indicate liver health).
      • Normal bilirubin levels (a substance made during the breakdown of red blood cells).
    • Coagulation (blood clotting) function:
      • Normal INR or PT (tests that measure how well your blood clots), unless on blood thinners.
      • Normal PTT (another test for blood clotting), unless on blood thinners.
  • Female patients who can have children must have a negative pregnancy test within 72 hours before starting the study and must not be breastfeeding.
  • Male and female patients who can have children must agree to avoid heterosexual sex or use acceptable birth control methods during the study and for 120 days after the last dose.
  • Willingness and ability to follow the study visit schedule and comply with all study procedures, as judged by the study doctor.
  • Must be at least 18 years old at the time of signing informed consent.
  • Must have a confirmed diagnosis of Head and Neck Squamous Cell Carcinoma (HNSCC) that is recurrent or metastatic and cannot be cured by local treatments.
  • The primary tumor must be located in the oral cavity, oropharynx, hypopharynx, or larynx.
  • Consent to provide the most recent tumor tissue sample for testing.
  • Confirmed PD-L1 CPS of 20 or more, as tested on the most recent tumor tissue sample.
  • Confirmed HPV tumor status for oropharyngeal cancer, as tested on the most recent tumor tissue sample. Testing is not required for oral cavity, hypopharynx, and larynx cancer.
  • Must have measurable disease according to specific guidelines. Tumors previously treated with radiation or other local therapies are considered measurable only if disease progression is clearly documented after treatment.
  • ECOG PS score of 0-1, which is a scale used to assess how a patient’s disease is progressing and how the disease affects their daily living abilities.

Who Cannot Join the Study?

  • Patients with medical conditions other than Head and Neck Squamous Cell Carcinoma cannot participate. This is a type of cancer that affects certain areas of the head and neck.
  • Patients who are not within the specified age range cannot participate. The age range is typically defined in the study details.
  • Patients who are part of a vulnerable population cannot participate. Vulnerable populations include groups that may need special protection, like children or those unable to give consent.
  • Patients who do not meet other specific health criteria set by the study cannot participate. These criteria are usually related to the patient’s overall health and medical history.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Hospital Universitario Y Politecnico La Fe Valencia Spain
Hospital Universitario De Navarra Pamplona Spain
Centre Jean Perrin Clermont Ferrand France

Other Sites

Site Name City Country Status
Istituto Europeo Di Oncologia S.r.l. Milan Italy
Hospital General Universitario Gregorio Maranon Madrid Spain
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Vitaz Sint-Niklaas Belgium
Oncolab S.R.L. Craiova Romania
Complex Oncological Center Plovdiv EOOD Plovdiv Bulgaria
MD Anderson Cancer Center Madrid Spain
Institutul Oncologic Prof. Dr. Alexandru Trestioreanu Bucuresti Bucharest Romania
Multiprofile Hospital For Active Treatment-Uni Hospital Ltd. Panagyurishte Bulgaria
Hospital Quironsalud Barcelona Barcelona Spain
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Fondazione IRCCS Policlinico San Matteo Pavia Italy
Hospital Clinic De Barcelona Barcelona Spain
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Universidade De Santiago De Compostela Santiago De Compostela Spain
Uniteversity Muliprofile Hospital For Active Treatment Tsaritsa Yoanna-Isul EAD Sofia Bulgaria
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca Cluj Napoca Romania
Hopitaux Prives De Metz Vantoux France
Vrije Universiteit Brussel Jette Belgium
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Provita Centrum Medyczne Sp. z o.o. Tomaszow Mazowiecki Poland
Multispecialty hospital for active treatment Sveta Sofia EOOD Sofia Bulgaria
Cmhctm Lvuf Bnmuot Lyon France
Itlkludj Cjfzvq Dgrkbhzyfraehvcaz L'hospitalet De Llobregat Spain
Ppoufxazhyi Lsfhyyhu &rmgakjhnjdaqpxhpqia Rddpt Klpnrdzooip Konin Poland
Cjz dgtjqxhtoeimqi Epagny Metz Tessy France
Nvorbjmx Iztknqaf Ouozivofm Iwh Mbjuy Soobghkvmysruuniqefpydesjhks Ipnazdxv Byxgpkkk Cracow Poland
Ugmolrqfqj Of Ajljdml Edegem Belgium
Cgxzpj Onyvq Lldvjvt Lille France
Hnbkrhen Umjnmjywbvkug dd A Cgbewy A Coruna Galicia Spain
Uhkyzcgojq Sxepjjcttrm Hypuekaa Fcf Auguvq Tastpcvnu Id Oojcqkmg Eff Sofia Bulgaria

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
01.01.2025
Bulgaria Bulgaria
Not recruiting
01.01.2025
France France
Not recruiting
01.01.2025
Italy Italy
Not recruiting
01.01.2025
Poland Poland
Not recruiting
01.01.2025
Romania Romania
Not recruiting
01.01.2025
Spain Spain
Not recruiting
01.01.2025

Trial locations

INBRX-106 is an investigational medication being studied for its potential to help the immune system fight cancer. It is being tested in combination with another medication to see if it can improve treatment outcomes for patients with certain types of head and neck cancer.

Pembrolizumab is a medication that helps the immune system attack cancer cells. It is already used to treat various types of cancer, including head and neck cancer. In this study, it is being used alone and in combination with another investigational medication to see which approach is more effective.

Head and Neck Squamous Cell Carcinoma – This is a type of cancer that originates in the squamous cells lining the moist surfaces inside the head and neck, such as the mouth, nose, and throat. It typically begins as a small, localized growth or sore that does not heal. As the disease progresses, it can invade nearby tissues and spread to lymph nodes in the neck. Symptoms may include a persistent sore throat, difficulty swallowing, and changes in voice. Over time, the cancer can spread to other parts of the body, leading to more complex symptoms. Early detection is crucial for managing the disease effectively.

Trial ID:
2024-515538-34-00
Protocol code:
INBRX106-01-201
Trial Phase:
Therapeutic use (Phase IV)

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