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Study of Monalizumab and Cetuximab in Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck
Not Recruiting
Trial ID: NCT02643550
Purpose
The objective of this study is to evaluate in a 3 +3 design, the safety of escalating doses
of Monalizumab given IV in combination with cetuximab in patients who have received prior
systemic regimen(s) for recurrent and/or metastatic squamous cell carcinoma of the head and
neck (SCCHN).
Cohorts expansion will evaluate antitumor activity of monalizumab and cetuximab with or
without anti-PD(L)1
Official Title
Phase 1b/2 Trial of IPH2201 And Cetuximab in Patients With Human Papillomavirus (HPV) (+) and HPV (-) Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck
Stanford Investigator(s)
A. Dimitrios Colevas, MD
Professor of Medicine (Oncology) and, by courtesy, of Otolaryngology - Head & Neck Surgery (OHNS) and of Radiation Oncology (Radiation Therapy)
Eligibility
Main Inclusion Criteria:
1. Age ≥ 18 years
2. Histologically or cytologically-confirmed, HPV (+) or HPV (-) squamous cell carcinoma
of the nasopharynx (WHO Type 1), oropharynx, hypopharynx, larynx (supraglottis,
glottis, subglottis) or oral cavity.
3. Recurrent or metastatic disease, documented by imaging (CT scan, MRI, X-ray) and/or
physical examination with measurable disease as per Response Evaluation Criteria in
Solid Tumors [RECIST] 1.1
For phase II cohorts:
- Cohort #1: Patients who received a maximum of two prior systemic regimens for
recurrent and/or metastatic disease and not amenable to further therapy with curative
intent
- Cohort #2: Patients with R/M SCCHN not amenable to therapy of curative intent, who
have received a maximum of two prior systemic regimens in the R/M setting and who have
received prior PD-(L)1 blockers
- Cohort #3: Patients with R/M SCCHN who have not received prior systemic regimens in
the R/M setting and who have not received prior PD-(L)1 inhibitors
Main Exclusion Criteria:
1. For phase II cohort #1 and cohort #2: Patients who received more than 2 prior systemic
regimens for recurrent and/or metastatic disease (no restriction in the phase Ib part
of the trial).
2. For phase II cohort #1 and cohort #2: Patients who received cetuximab or another
inhibitor of epidermal growth factor receptor are excluded from the phase II of the
trial, except if cetuximab was given as part of a primary treatment approach, with no
progressive disease for at least 4 months following the end of prior cetuximab
treatment.
Intervention(s):
biological: CETUXIMAB
biological: Monalizumab
biological: Anti-PD(L)1
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305
Michelle Jun
650-721-4079