Phase 3 study comparing ivonescimab alone or ivonescimab with ligufalimab versus pembrolizumab for the first-line treatment of recurrent and/or metastatic squamous cell carcinoma of the head and neck

Overview

Sponsor-declared trial summary

Key facts

Sponsor

Groupe Oncologie Radiotherapie Tete Cou

Participant type

Healthy volunteers

Age range

18-64 years, 65+ years

Gender

Male and Female

Therapeutic area

Diseases [C] - Neoplasms [C04]

Trial duration

5 May 2026 → ongoing

Decision date (initial)

2025-12-19

Transition trial

No

Low-intervention

No

Rare-disease indication

No

Vulnerable population

No

Trial design

CTIS Part I — objectives, methods, condition coding

Main objective

Scope: Therapy, Efficacy, Safety

To compare the Overall Survival (OS) of ivonescimab in combination with ligufalimab to Standard Of Care (SOC) pembrolizumab and ivonescimab to pembrolizumab in patients with 1 L R/M HNSCC PD-L1 positive (CPS ≥ 1).

Secondary objectives 7

1. To compare the objective response rate assessed by Blinded Independent Review Committee based on Response Evaluation Criteria in Solid Tumours (RECIST) v1.1 for ivonescimab in combination with ligufalimab to pembrolizumab and for ivonescimab to pembrolizumab
2. To compare the Progression free survival assessed by Blinded Independent Review Committee based on Response Evaluation Criteria in Solid Tumours (RECIST) v1.1 for ivonescimab in combination with ligufalimab to pembrolizumab and for ivonescimab to pembrolizumab
3. To compare the disease control rate, and duration of response as assessed by investigator, based on RECIST v1.1 for ivonescimab in combination with ligufalimab to pembrolizumab and for ivonescimab to pembrolizumab
4. To compare the safety and tolerability of ivonescimab in combination with ligufalimab to pembrolizumab and for ivonescimab to pembrolizumab.
5. To evaluate the pharmacokinetic (PK) profile and perform exposure/response analysis of ivonescimab.
6. To evaluate the immunogenicity of ivonescimab and ligufalimab.
7. To evaluate the PK profile and perform exposure/response analysis of ligufalimab.

Conditions and MedDRA coding

recurrent and/or metastatic squamous cell carcinoma of the head and neck

Eligibility criteria

Principal inclusion / exclusion criteria as submitted by sponsor

Inclusion criteria 11

1. Patient capable of voluntary giving her/his written informed consent.
2. Age ≥ 18 and < 80 years old at the time of enrolment
3. Eastern Cooperative Oncology Organization (ECOG) performance status score of 0 or 1.
4. Expected survival ≥ 6 months at randomization.
5. Histologically and/or cytologically confirmed R/M HNSCC with a primary tumour initially or currently located in the oral cavity, oropharynx, hypopharynx, or larynx.
6. HPV status test results based on tumour tissue samples must be obtained prior to randomization for patients with oropharyngeal cancer.
7. No prior systemic anti-tumour therapy for R/M HNSCC. Note: Patients who have previously received adjuvant/neoadjuvant chemotherapy with curative intent for non-metastatic disease, radiotherapy, or definitive radiotherapy in combination with chemotherapy or cetuximab/EGFR based therapy for locally advanced disease are eligible if disease progression occurs > 6 months after the end of the last treatment.
8. At least one measurable lesion according to RECIST v1.1, or measurable lesion with clear radiographic progression after local therapy, and the lesion must be suitable for repeated accurate measurements.
9. Tumours must be PD-L1 positive (CPS ≥ 1) as confirmed by CE-IVD immunohistochemistry assay based on local assessment with any assay validated for HNSCC in a laboratory compliant with National provisions. The measurement of PD-L1 protein expression can be performed based on archival tissue sample before the diagnosis of R/M tumour or based on tissue sample obtained after the diagnosis of a R/M tumour.
10. Adequate organ function determined by the following requirements: a. Haematology (satisfactory laboratory test results obtained during the screening period, and no blood components used within 14 days of cell growth factor supportive therapy): i. Absolute neutrophil value (ANC) ≥ 1.5×109/L (1,500/mm3) ii. Platelet count ≥ 100×109/L (100,000/mm3) iii. Haemoglobin ≥ 10 g/dL b. Kidneys: i. Calculated creatinine clearance ≥ 50 mL/min ii. Urine protein ≤ 2+ or 24 hours (h) urine protein quantification < 1.0 g c. Liver: i. Serum total bilirubin ≤ 1.5× upper limit of normal (ULN); for patients with liver metastases or confirmed/suspected Gilbert syndrome, ≤ 3 × ULN ii. AST and ALT ≤ 2.5×ULN; For patients with liver metastases, AST and ALT ≤ 5×ULN iii. Serum albumin ≥ 28 g/L d. Coagulation function: International normalized ratio (INR) and/or activated partial thromboplastin time (APTT) ≤ 1.5× ULN. This applies only to patients who are not on therapeutic anti- coagulation. Patients receiving therapeutic anti-coagulation should be on a stable dose.
11. Patient is willing and able to comply with the visits, treatment protocols, laboratory tests, and other requirements of the study as specified in the schedule.

Exclusion criteria 14

1. Primary tumour site (any histology) of nasopharynx, nasal cavity, sinuses, salivary glands, thyroid or parathyroid glands, skin, or unknown primary site of tissue origin.
2. Patient with malignancies other than HNSCC within 3 years prior to enrolment. Patients with other tumours that have been cured through local treatment, such as basal or cutaneous squamous cell carcinoma, superficial bladder cancer, cervical or breast carcinoma in situ, are not excluded.
3. Concurrent enrolment in another clinical study, unless it is an observational, non-interventional clinical study or a follow-up period of an interventional study; Received study treatment within 4 weeks prior to randomization.
4. Prior treatment with systemic anti-angiogenic drugs.
5. Previous head and neck re-irradiation for recurrent/metastatic disease
6. Prior immunotherapy, including immune checkpoint inhibitors (e.g., anti-PD-1/L1 antibody, anti- CTLA-4 antibody, anti-TIGIT antibody, anti-LAG3 antibody, anti-CD47, anti-SIRPα, etc.), immune checkpoint agonists (e.g., ICOS, CD40, CD137, GITR, OX40 antibodies, etc.), immune cell therapy, and any other treatment that targets tumour immunity including therapeutic tumour vaccine, and other adjuvant/neoadjuvant anti-PD-1 based therapy.
7. Patients with ulcers on the skin surface related to the current cancer during the screening period, superficial or protruding skin lesions with excessive surface tension and a greater risk of ulceration, or other patients with a greater risk of ulceration as assessed by the investigator. Patients with recent tracheostomy involving the tumour which are at risk of bleeding.
8. Imaging during the screening period shows that the tumour invades/infiltrates the surrounding important organs (such as trachea, oesophagus, and based on investigator assessment of bleeding risk) and/or large blood vessels in the neck (such as subclavian artery, common internal and/or external carotid artery, c, etc.) or if the investigator judges that entering the study might cause a potential risk of bleeding.
9. Presence of brainstem, meningeal metastases, spinal cord metastases or compression, or leptomeningeal disease. 10. Received curative head and neck radiotherapy within 6 months prior to randomization. Palliative local treatment for non-head and neck areas carried out within 3 weeks before randomization; Received non-specific immunomodulatory therapy (such as interleukin, interferon, thymus peptide, tumour necrosis factor, etc.) within 2 weeks prior to randomization, excluding IL-11 for the treatment of thrombocytopenia.
10. Received curative head and neck radiotherapy within 6 months prior to randomization. Palliative local treatment for non-head and neck areas carried out within 3 weeks before randomization; Received non-specific immunomodulatory therapy (such as interleukin, interferon, thymus peptide, tumour necrosis factor, etc.) within 2 weeks prior to randomization, excluding IL-11 for the treatment of thrombocytopenia.
11. Presence of active autoimmune disease requiring systemic therapy (e.g., treatment with disease-modifying drugs, corticosteroids, immunosuppressants) within 2 years prior to randomization. Alternative therapies (e.g., thyroxine, insulin, or those targeting the adrenal glands or pituitary) and physiologic corticosteroid replacement therapy for pituitary insufficiency are not considered systemic treatment.
12. Patients with known active tuberculosis and suspected active tuberculosis need to be excluded by clinical examination; Known active syphilis infection.
13. Severe infection within 4 weeks prior to randomization, including but not limited to comorbidities requiring hospitalization History of immunodeficiency; Those who have history of positive test for HIV antibodies; Current long-term use of systemic
14. sepsis, or severe pneumonia; Active non-severe infection that has received systemic anti-infective therapy within 2 weeks prior to randomization.

Endpoints

Primary and secondary outcome measures (English text)

Primary endpoints 1

1. Overall Survival

Secondary endpoints 6

1. Objective response rate
2. Progression free survival
3. Disease control rate
4. safety assessments
5. pharmacokinetic characteristics
6. Immunogenicity assessment

Investigational products

Investigational medicinal products (IMPs), comparators, placebo, auxiliary

Test 3

Comparator 1

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Groupe Oncologie Radiotherapie Tete Cou

Sponsor organisation

Groupe Oncologie Radiotherapie Tete Cou

Address

4 B Rue Emile Zola

City

Tours

Postcode

37000

Country

France

Scientific contact point

Organisation

Groupe Oncologie Radiotherapie Tete Cou

Contact name

Aurore Vozy

Public contact point

Organisation

Groupe Oncologie Radiotherapie Tete Cou

Contact name

Adeline PECHERY

Sponsor responsibilities

Article 77 compliance

Groupe Oncologie Radiotherapie Tete Cou

Contact point sponsor

Groupe Oncologie Radiotherapie Tete Cou

Article 77 implementation

Groupe Oncologie Radiotherapie Tete Cou

Locations

3 EU/EEA countries · 51 investigational sites

By country

Investigational sites

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Results and documents

Annex IV summary of results, Annex V layperson summary, and all documents registered in CTIS for this trial

Documents 29 files

Public protocol annexes, IB summaries, regulatory submissions and post-authorisation documents registered in CTIS.

Application history

4 submissions — initial application plus substantial / non-substantial modifications