Study of petosemtamab compared to standard therapy in previously treated patients with metastatic or recurrent head and neck cancer

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What is this study about?

This study focuses on treating head and neck squamous cell carcinoma that has spread to other parts of the body (metastatic) or has come back (recurrent) and cannot be cured. The study will test a new medication called petosemtamab and compare it to other standard treatments that may include methotrexate, docetaxel, or cetuximab.

The purpose of this research is to determine if petosemtamab is more effective than currently available treatments in helping patients with head and neck cancer live longer and to see how well tumors respond to the treatment. The study is designed for patients whose cancer has continued to grow despite previous treatment with platinum-containing therapy and immune therapy.

During the study, participants will be randomly assigned to receive either petosemtamab or one of the standard treatments. All medications will be given through an intravenous infusion. The treatment period will last up to 6 months, depending on how well the treatment works and how well it is tolerated. Throughout the study, patients will have regular check-ups to monitor their health and assess how their cancer responds to treatment.

1 Initial assessment

Your doctor will assess if you have head and neck cancer that has spread or come back after previous treatments.

The cancer must be in one of these areas: oropharynx, oral cavity, hypopharynx, or larynx.

You must have previously received platinum therapy and anti-PD-1 treatment.

Your overall health status will be evaluated, including organ function and physical capability.

2 Treatment assignment

You will be randomly assigned to receive either petosemtamab or another treatment chosen by your doctor.

The other treatment options may include methotrexate, docetaxel, or cetuximab.

All medications will be given through an intravenous infusion (directly into your vein).

3 Treatment period

You will receive regular treatments according to your assigned medication schedule.

Your doctor will monitor how your cancer responds to treatment using imaging scans.

Regular health assessments will check for any side effects or complications.

Treatment will continue as long as it is helping and side effects are manageable.

4 Follow-up period

After treatment ends, you will have regular check-ups to monitor your health.

Doctors will track how long the treatment effects last.

The study will continue until March 2028.

Who Can Join the Study?

  • Must be 18 years or older and able to provide informed consent
  • Must have confirmed head and neck squamous cell carcinoma (a type of cancer) that has spread or is locally advanced and cannot be cured with standard therapy
  • Cancer must be located in one of these areas: oropharynx (back of the throat), oral cavity (mouth), hypopharynx (lower throat), or larynx (voice box)
  • Must have previously received and progressed after treatment with anti-PD-1 therapy (a type of immunotherapy) and platinum-containing therapy (a type of chemotherapy)
  • Must have measurable disease that can be evaluated by imaging scans
  • Must have good physical function with an ECOG score of 0 or 1 (able to perform daily activities with minimal assistance)
  • Must have a life expectancy of at least 12 weeks
  • Must have adequate organ function as specified in the protocol
  • Must be willing to provide a new tumor biopsy or existing tumor tissue sample
  • For patients with oropharyngeal cancer, must have documentation of p16 status (a specific tumor marker test)
  • Cannot have had previous anti-EGFR therapies, except if cetuximab was used with radiation therapy more than 1 year ago
  • HIV-positive patients may participate if they have a CD4+ count of 300 or higher, undetectable viral load, and are receiving HIV treatment

Who Cannot Join the Study?

  • Prior history of squamous cell carcinoma (a type of skin cancer) in areas other than head and neck
  • Active brain or spinal cord metastases (cancer that has spread to these areas) that are untreated or unstable
  • Previous treatment with experimental medications within 28 days before starting this study
  • Known severe allergic reactions to biological treatments or drugs
  • Presence of active, clinically significant infections requiring systemic treatment
  • Major surgery within 28 days before starting the study treatment
  • Significant heart problems including uncontrolled high blood pressure, unstable heart disease, or heart failure
  • Active autoimmune disease requiring systemic treatment
  • Other active cancers requiring treatment (except for adequately treated non-melanoma skin cancer or cervical cancer in situ)
  • Pregnant or breastfeeding women
  • Known infection with HIV, Hepatitis B, or Hepatitis C
  • Any medical condition that, in the investigator’s opinion, would make participation unsafe

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
Asklepios Kliniken Hamburg GmbH Hamburg Germany
Centre Antoine Lacassagne Nice France
Diagnostic & Therapeutic Center Of Athens Hygeia Single Member S.A. Athens Greece
Hopitaux Universitaires Pitie Salpetriere Paris France
Centrum Onkologii Im. Prof. Franciszka Lukaszczyka W Bydgoszczy Bydgoszcz Poland
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Centre hospitalier universitaire de Liege Liege Belgium
Universitair Ziekenhuis Gent Gent Belgium
Universitaetsklinikum Aachen AöR Aachen Germany
Hospital Universitario 12 De Octubre Madrid Spain
Fundacion Instituto Valenciano De Oncologia Valencia Spain
Lietuvos sveikatos mokslu universiteto ligonine Kauno klinikos Kaunas Lithuania
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Hospital Cuf Descobertas S.A. Lisbon Portugal
University General Hospital Of Heraklion Heraklion Greece
Hospital Quironsalud Barcelona Barcelona Spain
Centre Henri Becquerel Rouen France
Universitair Medisch Centrum Utrecht Utrecht The Netherlands
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Universitaetsklinikum Mannheim GmbH Mannheim Germany
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz Nyiregyhaza Hungary
Nemocnice AGEL Novy Jicin a.s. Novy Jicin Czechia
General University Hospital Of Patras Patras Greece
Justus-Liebig-Universitaet Giessen Giessen Germany
St. Luke’s Hospital S.A. Thessaloniki Greece
University Hospital Olomouc Olomouc Czechia
Netherlands Cancer Institute Amsterdam The Netherlands
Universita Degli Studi Di Brescia Brescia Italy
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Stichting Radboud University Medical Center Nijmegen The Netherlands
Pratia S.A. Skorzewo Poland
University Of Pecs Pecs Hungary
Beskidzkie Centrum Onkologii Szpital Miejski Im. Jana Pawla II W Bielsku-Bialej SPZOZ Bielsko-Biala Poland
Clinique Victor Hugo Le Mans France
University Of Szeged Szeged Hungary
Centre De Lutte Contre Le Cancer Eugene Marquis Rennes France
University General Hospital Attikon General Hospital Of West Attica H Agia Varvara Chaidari Greece
Cpwawixvf Uwxkijjerhtyye Skinbbvgw Woluwe-Saint-Lambert Belgium
Iyxefnmb Rcysnxza Dz Cwqzwt Dl Miueaiaqfgj Montpellier France
Clktea Lzaq Basoex Lyon France
Uqqlowmcls Mpwrrsv Cgbuww Hwpqpqmrynrsdndny Hamburg Germany
Uqftfreuthlexejyremjp Enzcc Axx Essen Germany
Wtqseysetfb Wwwtunmfvresvhlifnww Cyaforc Oddttbaef I Tnpoxwteoqzdc Iq Mwlnzwmczvz W Lvfvl Lodz Poland
Alqucvnuzw Pjyeqpct Hnxnvurw Dc Mlfmayqhe Marseille France
Cnlhjr Hjsgbgtqch E Uqsrfjokpgcvk Dq Clrrxnz Ebuieu Coimbra Portugal
Ujhdgktcepxjur Cdijpfd Kjqefqztu Gdansk Poland
Ffdcgwdn nsjamlvlq Msdqh a Hqgohvt Prague Czechia
Uelepfaoza Dxlyh Syayu Dq Rgvk Lf Socgvxvl Rome Italy
Nebqtufl Ivnkwvro Oiwgugtrd Iho Mpsxr Spwtlfepnjpdajkzbqommxwgzgfw Iautyrpp Bpltoghd Cracow Poland
Umxnazubkukcukllibkzr Wapjsuvpd Aqk Wuerzburg Germany
Vimlfcbch ihzvgvpi Vgvuwugv ubtfbifyasdj lphgwpkge Sblflsqi kkluvfc faivwaua Nrrnxhoscwex vbyyi coexcwj Vilnius Lithuania
Hiozjbrv Vwuc dvbmclzd Barcelona Spain
Chywni Okgcb Lydpqma Lille France

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Recruiting
15.08.2024
Czechia Czechia
Recruiting
15.08.2024
France France
Recruiting
15.08.2024
Germany Germany
Recruiting
15.08.2024
Greece Greece
Recruiting
15.08.2024
Hungary Hungary
Recruiting
15.08.2024
Italy Italy
Recruiting
15.08.2024
Lithuania Lithuania
Recruiting
15.08.2024
Poland Poland
Recruiting
15.08.2024
Portugal Portugal
Recruiting
15.08.2024
Spain Spain
Recruiting
15.08.2024
The Netherlands The Netherlands
Recruiting
15.08.2024

Trial locations

Petosemtamab is an investigational medication being studied for treating head and neck cancer that has spread or come back after previous treatments. It works by targeting specific proteins on cancer cells to help fight the disease.

Investigator’s choice monotherapy refers to a single medication chosen by the doctor from a set of approved treatment options. This allows the doctor to select the most appropriate standard treatment for each patient based on their individual case.

Both treatments are being compared to see which one is more effective at helping patients with head and neck cancer who have already tried other treatments, including platinum chemotherapy and immunotherapy (anti-PD-1 therapy), but whose cancer has continued to grow or spread.

Head and Neck Squamous Cell Carcinoma (HNSCC) – A type of cancer that begins in the squamous cells that line the moist surfaces inside the head and neck regions. The disease typically develops in the mucous membranes of the mouth, nose, and throat. It can spread (metastasize) to other parts of the body through the lymph system or bloodstream. The cancer can recur after initial treatment, appearing in the same area or spreading to other parts of the body. The condition affects the cells’ normal growth and division processes, causing them to multiply uncontrollably and form tumors.

Metastatic Cancer – A condition where cancer cells spread from their original location to other parts of the body. The process occurs when cancer cells break away from the primary tumor and travel through blood vessels or lymph vessels to form new tumors in other organs or tissues. These new tumors, called metastases, are the same type of cancer as the primary tumor. The spread can affect multiple organs simultaneously and represents an advanced stage of cancer development.

Recurrent Cancer – A form of cancer that returns after a period during which the cancer could not be detected. The cancer may come back to the same place as the original tumor or to another place in the body. The reappearance can happen months or years after the initial treatment. The returning cancer cells are the same type as the original cancer.

Trial ID:
2023-510322-32-00
Protocol code:
MCLA-158-CL02
Trial Phase:
Therapeutic confirmatory (Phase III)

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