A Study of Setanaxib Co-Administered With Pembrolizumab in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of Head and Neck (SCCHN)

Squamous Cell Carcinoma of Head and Neck Clinical Trial

Official title:

A Phase 2, Randomised, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Setanaxib, When Administered With Pembrolizumab, in Patients With Recurrent or Metastatic SCCHN

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05323656
• Other study ID #: GSN000400
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: April 6, 2022
• Est. completion date: September 2024

Study information

• Verified date: April 2024
• Source: Calliditas Therapeutics AB
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to compare the change in tumour size per Response Evaluation Criteria in Solid Tumours Version 1.1 (RECIST v1.1) in recurrent or metastatic SCCHN patients treated with setanaxib and pembrolizumab versus patients treated with placebo and pembrolizumab.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 55
• Est. completion date: September 2024
• Est. primary completion date: February 18, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female patients aged =18 years, inclusive, at the time of informed consent.

• Willing and able to give informed consent and to comply with the requirements of the study.

• Histologically- or cytologically-confirmed diagnosis of SCCHN that is recurrent or metastatic with or without nodal involvement, and with or without metastatic spread, and is not eligible for surgical resection.

• Candidates for first-line treatment for pembrolizumab for recurrent or metastatic SCCHN, at the discretion of the investigator.

• A positive CAFs level (defined as CAFs level in tumours =5%), performed at a central laboratory, with fresh tumour biopsy taken during or within 30 days prior to the Screening Period. If available, suitable archival tissue (taken within 6 months prior to the Screening Visit and where the patient has received no further anti-cancer therapy during this 6-month period) can be used to assess tumour CAFs level and determine patient eligibility.

• Measurable disease, in accordance with RECIST v1.1, and with tumour accessible and of sufficient volume for pre-treatment and on-treatment biopsy.

• Combined positive score (CPS) =1, as determined on the archival or fresh tumour biopsy taken during or within 30 days prior to the Screening Period.

• HPV status known at randomisation.

• Life expectancy of at least 6 months in the judgment of the investigator.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

• Adequate organ and bone marrow function within 35 days of starting study treatment. Criteria "a" to "c" cannot be met in patients with ongoing or recent (within 14 days of screening test) transfusions or who require ongoing growth factor support:

1. Absolute neutrophil count =1,000/mm3 (= 1.0×109/L).

2. Platelet count =100,000/mm3 (= 100×109/L).

3. Haemoglobin =9 g/dL, in the absence of transfusions for at least 2 weeks. Patients requiring ongoing transfusions or growth factor support to maintain haemoglobin = 9g/dL are not eligible.

4. Total bilirubin =1.5×upper limit of normal (ULN) (if associated with liver metastases or Gilbert's disease, =3×ULN).

5. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =3×ULN.

6. Serum creatinine =2.0 mg/dL or creatinine clearance =40 mL/min (measured or calculated according to the method of Cockcroft and Gault).

• Female patients of childbearing potential must use a highly effective method of contraception to prevent pregnancy for =4 weeks before randomisation and must agree to continue strict contraception up to 120 days after the last dose of IMP or pembrolizumab, whichever is the later.

1. For the purposes of this study, women of childbearing potential are defined as "fertile, following menarche and until becoming postmenopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy."

2. Postmenopausal state is defined as no menses for 12 months without an alternative medical cause. In female patients who are not using hormonal contraception or hormonal replacement therapy but with suspected menopause and less than 12 months of amenorrhea, a high follicle stimulating hormone (FSH) level in the postmenopausal range will be required at Screening to confirm a postmenopausal state. Confirmation with more than one FSH measurement is required.

3. Highly effective contraception is defined as methods that can achieve a failure rate of less than 1% per year when used consistently and correctly.

• Female patients of childbearing potential must have a negative serum pregnancy test at Screening and a negative urine pregnancy test at Baseline/Randomisation before dosing.

• Male patients with female partners of childbearing potential must be willing to use a condom and require their partner to use an a highly effective contraceptive method.

• Male patients must refrain from donating sperm, and female patients must refrain from donating eggs, from Baseline until 120 days after the last dose of IMP or pembrolizumab, whichever is the later.

Exclusion Criteria:

• Diagnosis of immunosuppression or receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of study treatment, with the exception of intranasal and inhaled corticosteroids or systemic corticosteroids at doses not to exceed 10 mg/day of prednisone or equivalent. Steroids as premedication for hypersensitivity reactions due to radiographic contrast agents are allowed.

• Anti-cancer mAb treatment within 4 weeks prior to study Day 1.

• Chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 (radiation therapy can be allowed for palliative therapy of bone metastasis only).

• Not recovered from AEs Grade 2 or greater (except for alopecia) due to previously administered agents.

• Treatment with any investigational agent within 12 weeks of Screening Visit or 5 half-lives of the IMP (if known), whichever is longer, or current enrolment in an interventional clinical study.

• Prior treatment with setanaxib or participation in a previous setanaxib clinical study.

• Prior treatment with pembrolizumab.

• Known additional malignancy that is progressing or requires active treatment excepting basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in situ cervical cancer that has undergone potentially curative therapy, or malignancy treated with curative intent and with no known active disease =2 years before the first dose of IMP and of low potential risk for recurrence.

• Known active central nervous system metastases and/or carcinomatous meningitis.

• Active autoimmune disease requiring systemic treatment within the past 3 months or documented history of clinically severe autoimmune disease, or syndrome that requires systemic steroids or immunosuppressive agents. The following are exceptions to this criterion:

1. Patients with vitiligo or alopecia.

2. Any chronic skin condition that does not require systemic therapy.

3. Patients with coeliac disease controlled by diet alone.

• Any evidence of current interstitial lung disease or pneumonitis, or a prior history of interstitial lung disease or non-infectious pneumonitis requiring high-dose glucocorticoids.

• Active infection requiring systemic therapy.

• Known human immunodeficiency virus (HIV) infection or acute or chronic hepatitis B or C infection. Patients with a past or resolved hepatitis B virus infection (defined as the presence of hepatitis B core antibody [HBcAb] and absence of hepatitis B surface antigen [HBsAg]) are eligible provided the hepatitis virus DNA test is negative. Patients positive for hepatitis C antibody are eligible only if polymerase chain reaction (PCR) is negative for hepatitis C virus RNA. Patients with ongoing anti-viral therapy with potent inhibitors of cytochrome P450 (CYP) 3A4 are not eligible. Testing for HIV is only required if clinically indicated and is not mandatory for this study.

• Serious chronic gastrointestinal conditions associated with diarrhoea.

• History of significant haematological problems, such as blood dyscrasias requiring treatment, aplastic anaemia, myelodysplastic syndrome, or leukaemia.

• Surgery (eg, stomach bypass) or medical condition that might significantly affect absorption of medicines (as judged by the investigator).

• A positive pregnancy test or breastfeeding for female patients.

• Evidence of any of the following cardiac conduction abnormalities: a QTc Fredericia interval >450 milliseconds for male patients or >470 milliseconds for female patients. Patients with a second- or third-degree atrioventricular block are to be excluded.

• TSH >ULN at Screening.

• Unstable cardiovascular disease as defined by any of the following:

1. Unstable angina within 6 months prior to Screening

2. Myocardial infarction, coronary artery bypass graft surgery, or coronary angioplasty within 6 months prior to Screening

3. Cerebrovascular accident within 6 months prior to Screening

4. New York Heart Association Class III or IV heart failure

• Presence of any laboratory abnormality or condition that, in the opinion of the investigator, could interfere with or compromise a patient's treatment, assessment, or compliance with the protocol and/or study procedures.

• Any other condition that, in the opinion of the investigator, constitutes a risk or contraindication for the participation of the patient in the study, or that could interfere with the study objectives, conduct, or evaluation.

• Use of medications known to be potent CYP3A4 inhibitors or inducers, or potent uridine diphosphate (UDP)-glucuronosyltransferase 1A9 (UGT1A9) inhibitors or inducers, within 21 days prior to IMP administration.

• Legal incapacity or limited legal capacity.

• Psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.

• Patients who are unable to provide informed consent, are incarcerated or unable to follow protocol requirements.

• Previous randomisation in this study.

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Squamous Cell
• Squamous Cell Carcinoma of Head and Neck

Intervention

Drug:
• Setanaxib
Oral tablets, 400 mg per tablet

Biological:
• Pembrolizumab
200 mg IV infusion

Drug:
• Placebo
Oral tablets

Locations

Country	Name	City	State
France	Centre Hospitalier Universitaire Amiens-Picardie - Site Sud	Amiens Cedex 1	Picardie
France	Ramsay Health Clinic Belharra	Bayonne
France	Hôpital Saint-André	Bordeaux
France	Centre de Lutte contre le Cancer - Centre Oscar Lambret	Lille	Hauts-de-France
France	Centre Léon Bérard	Lyon
France	Hôpital de la Timone	Marseille
France	Institut Régional du Cancer de Montpellier	Montpellier
France	Institut de Cancérologie de Lorraine	Vandœuvre-lès-Nancy	Grand Est
Germany	Medizinische Hochschule Hannover	Hannover	Niedersachsen
Italy	Azienda Socio-Sanitaria Territoriale Santi Paolo e Carlo - Ospedale San Paolo Polo Universitario	Milano	Milan
Italy	Fondazione Policlinico Universitario Agostino Gemelli IRCCS	Roma
Poland	Centrum Onkologii Im. Prof. F. Lukaszczyka w Bydgoszczy	Bydgoszcz	Kujawsko-pomorskie
Poland	Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie-Panstwowy Instytut Badawczy O. w Gliwicach	Gliwice	Slaskie
Spain	Hospital Clínic de Barcelona	Barcelona
Spain	Hospital Universitario La Paz	Madrid
Spain	Complejo Hospitalario de Navarra	Pamplona
Spain	Hospital Universitario Virgen del Rocío	Sevilla
United Kingdom	The Royal Marsden Hospital - London	London	England
United Kingdom	The Royal Marsden Hospital Head and Neck Unit	Sutton	England
United States	Siteman Cancer Center - West County	Creve Coeur	Missouri
United States	Siteman Cancer Center - North County	Florissant	Missouri
United States	Mount Sinai Comprehensive Cancer Center	Miami Beach	Florida
United States	Washington University School of Medicine Center for Advanced Medicine	Saint Louis	Missouri
United States	Siteman Cancer Center - St. Peters	Saint Peters	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Calliditas Therapeutics Suisse SA

Countries where clinical trial is conducted

United States,  France,  Germany,  Italy,  Poland,  Spain,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Best Percentage Change in Tumour Size	Defined as the best percentage change from Baseline in the sum of diameters of target lesions, as assessed by RECIST v1.1.	Baseline up to approximately 26 months
Secondary	Progression Free Survival (PFS)	Defined as time from randomisation to the first documented disease progression per RECIST v1.1 or death due to any cause, whichever occurs first.	Baseline up to approximately 21 months
Secondary	Change From Baseline in Cancer-associated Fibroblasts (CAFs) Level in Tumour Tissue		Baseline up to approximately 26 months
Secondary	Change From Baseline in the Number of Cluster of Differentiation 8 (CD8+) Tumour Infiltrating Lymphocytes (TILs) in Tumour Tissue		Baseline up to approximately 26 months
Secondary	Change From Baseline in the Number of Regulatory T-cells in Tumour Tissue		Baseline up to approximately 26 months
Secondary	Overall Response Rate (ORR)	Proportion of the patients who have a complete response (CR) or partial response (PR) per RECIST v1.1 will be used to access ORR.	Baseline up to approximately 26 months
Secondary	Duration of Response (DoR)	The minimum time when CR or PR is first observed to the time of progression of disease (PD) or death will be used to access DoR.	Baseline up to approximately 26 months
Secondary	Disease Control Rate (DCR)	Proportion of the patients in whom the best overall response is determined as CR, PR, or stable disease (SD) per RECIST v1.1 will be used to access DCR.	Baseline up to approximately 26 months
Secondary	Overall Survival (OS)	Defined as the time from randomisation to death due to any cause. Patients without documented death at the time of the final analysis will be censored at the date of the last follow-up.	Baseline up to approximately 26 months
Secondary	Number of Participants with Adverse Events (AEs)	Any clinically significant abnormalities in vital signs, physical examination, clinical laboratory tests (including biochemistry, hematology, urinalysis, and thyroid function), or 12- lead electrocardiogram (ECG) results will be recorded as Adverse Events (AEs).	Baseline up to approximately 26 months
Secondary	Number of Participants with Adverse Events of Special Interest (AESI)	AESI include Anaemia and Hypothyroidism.	Baseline up to approximately 26 months
Secondary	Levels of PD-L1 Expression in Tumour Tissue		Baseline up to approximately 26 months
Secondary	Quantification of Gene Expression Related to CAFs		Baseline up to approximately 26 months
Secondary	Quantification of Gene Expression Related to CD8+ TILs		Baseline up to approximately 26 months
Secondary	Quantification of Gene Expression Related to Regulatory T-cells		Baseline up to approximately 26 months
Secondary	Area Under The Concentration-time Curve Over a 24-hour Period at Steady State (AUC[0-24]-ss) of Setanaxib		Baseline up to approximately 26 months
Secondary	Area Under The Concentration-time Curve Over a 24-hour Period at Steady State (AUC24-ss) of GKT138184		Baseline up to approximately 26 months
Secondary	Minimum Serum Concentration at Steady State (Cmin-ss) of Setanaxib		Baseline up to approximately 26 months
Secondary	Minimum Plasma Concentration at Steady State (Cmin-ss) of GKT138184		Baseline up to approximately 26 months
Secondary	Maximum Serum Concentration at Steady State (Cmax-ss) of Setanaxib		Baseline up to approximately 26 months
Secondary	Maximum Serum Concentration at Steady State (Cmax-ss) of GKT138184		Baseline up to approximately 26 months