A Clinical Study to Assess the Efficacy of Adjuvant Immunotherapy With Cemiplimab in Patients With Surgically Removed Non-small Cell Lung Cancer Who Have Not Received Prior Chemotherapy

Recruiting now · Phase 3

Conditions studied: Non-Small Cell Lung Cancer

In brief

ARCH is a randomised, stratified, multicentre, phase III trial. Protocol treatment consists of cemiplimab, 350 mg i.v., every 3 weeks, for 4 cycles, followed by 700 mg i.v., every 6 weeks for 6 cycles or until relapse or unacceptable toxicities, whichever occurs first. The primary objective of the study is to determine the efficacy of adjuvant cemiplimab, as measured by disease-free survival, in patients without prior adjuvant platinum-based chemotherapy, compared to observation without adjuvant treatment. The primary objective will be assessed in patients with tumours with centrally confirmed PD-L1 expression of ≥1%.

Key facts

Study ID

NCT06931717

Run by

ETOP IBCSG Partners Foundation

People needed

390

Starts

2026-01-12

Expected to finish

2029-03-01

Last updated by the study team

2026-07-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Pathological stage II-IIIA (UICC/ AJCC staging 9th edition) NSCLC Brain imaging should have been performed to complete staging, either preoperatively or postoperatively. If brain imaging has not been performed, a contrast-enhanced CT or MRI of the brain must be performed at screening prior randomisation.
• Complete resection with negative surgical margins (R0).
• Acceptable types of surgical resection include any of the following:
• Lobectomy, sleeve lobectomy, bilobectomy, or pneumectomy.
• Segmentectomy for tumours ≤2 cm is permitted in patients with poor pulmonary reserve or another major comorbidity that contraindicates lobectomy.
• Wedge resection is not allowed.
• Lymph node dissection should be done according to applicable guidelines.
• No disease recurrence following surgical resection.
• Tumour PD-L1 expression of ≥1%, determined locally using a locally approved immuno-histochemistry test.
• Availability of archival FFPE tumour tissue for central PD-L1 expression testing.
• Patient is not considered for adjuvant platinum-based chemotherapy due to:
• Documented patient refusal; or
• Patient is unfit to receive adjuvant platinum-based chemotherapy (per investigator assessment) due to:
• ECOG PS2, or ECOG PS 0/1 and aged ≥70 years with substantial comorbidities or other contraindication(s) to platinum-based doublet chemotherapy.
• Estimated life expectancy of ≥3 months.
• Age ≥18 years.
• Patient has recovered from surgery-related complications.
• Adequate haematological, renal and liver function.
• Patient is able to comply with the trial protocol, in the investigator's judgment.
• Negative pregnancy test Female participants of childbearing potential (including women who had their last menstruation in the last 2 years), must have a negative serum pregnancy test within 5 weeks before randomisation. Pregnancy test must be repeated within 3 days before the first dose of protocol treatment and at every treatment visit (urine beta HCG test is sufficient).
• Use of highly effective contraceptive methods Female participants of childbearing potential (including women who had their last menstruation in the last 2 years) and male participants with a female partners of childbearing potential must agree to use a highly effective method of contraception for the duration of the protocol treatment and until 4 months after the last dose of cemiplimab.
• Written Informed Consent must be signed and dated by the patient and the investigator prior to any trial-related intervention.

You may not qualify if…

• EGFR-mutant or ALK-rearranged NSCLC.
• Any small cell component
• Prior neoadjuvant and/or adjuvant systemic treatment for NSCLC.
• Note: Previous treatment for another malignancy not excluded as per next criterion (Participating in another interventional clinical trial for NSCLC) is allowed if the below conditions are fulfilled:
• Treatment with an approved systemic therapy is completed >4 weeks before randomisation or
• Treatment with systemic biologic therapy is completed >5 half-lives before randomisation and patient has recovered from any immune-mediated adverse events and endocrinopathies are adequately managed with hormone replacement.
• Participating in another interventional clinical trial for NSCLC.
• Diagnosis with another malignancy other than NSCLC that is progressing or requires active treatment.
• Exceptions:
• Non-melanoma skin cancer that has undergone potentially curative therapy
• In situ cervical carcinoma
• Any tumour that has been deemed to be definitively treated, such as definitively treated non-metastatic prostate cancer.
• Has any condition requiring ongoing/continuous corticosteroid therapy (>10 mg prednisone/day or anti-inflammatory equivalent) within 1 week prior to randomisation. Physiologic replacement doses are allowed even if they are >10 mg of prednisone per day or equivalent, as long as they are not being administered for immunosuppressive intent. Inhaled or topical steroids are permitted, provided that they are not for treatment of an autoimmune disorder.
• Note: Patients who require a brief course of steroids (ex. 3 days in the week before randomisation) or physiologic replacement are allowed to be included in the study.
• Ongoing or recent (within 5 years) evidence of significant autoimmune disease that required treatment with systemic immunosuppressive treatments.
• The following are not exclusions: vitiligo, childhood asthma that has resolved, endocrinopathies (such as hypothyroidism or type 1 diabetes) that require only hormone replacement, or psoriasis that does not require systemic treatment.
• Encephalitis, meningitis, organic brain disease (e.g., Parkinson's disease) or uncontrolled seizures within 1 year prior to randomisation.
• Myocardial infarction within 6 months prior to randomisation.
• Known history of, or any evidence of, interstitial lung disease or active, non-infectious pneumonitis within 5 years prior to randomisation.
• Uncontrolled infection with HIV, hepatitis B, or hepatitis C infection; or the patient has a diagnosis of immunodeficiency.
• Patients with known HIV infection who have controlled infection [undetectable viral load (HIV RNA PCR) and CD4 count above 350 either spontaneously or on a stable antiviral regimen] are allowed to be included in the study. Patients with controlled HIV infection should be monitored according to local standards.
• Patients with hepatitis B (HBsAg+) with controlled infection (serum hepatitis B virus DNA PCR that is below the limit of detection and receiving antiviral therapy for hepatitis B) may be included in the study. Patients with controlled infection must undergo regular monitoring of HBV DNA. Patients must remain on antiviral therapy for at least 6 months after the last dose of cemiplimab.
• Patients who are hepatitis C virus antibody positive (HCV Ab+) with controlled infection (undetectable HCV RNA by PCR either spontaneously or in response to a successful prior course of anti-HCV therapy) may be included in the study.
• Any infection requiring hospitalisation or treatment with intravenous anti-infectives within 2 weeks before randomisation.
• Receipt of a live vaccine within 28 days before randomisation.

Where it is running

• Complejo Hospitalario Universitario — A Coruña, Spain (enrolling)
• Hospital General Universitario Dr. Balmis de Alicante — Alicante, Spain (enrolling)
• Hospital Universitario Cruces — Barakaldo, Spain (enrolling)
• Hospital de La Santa Creu I Sant Pau — Barcelona, Spain (enrolling)
• Hospital Universitario Vall D'Hebron — Barcelona, Spain (enrolling)
• Hospital Clínico San Cecilio de Granada — Granada, Spain (enrolling)
• Hospital Universitario de Jerez de La Frontera — Jerez de la Frontera, Spain (enrolling)
• Hospital Clínico San Carlos — Madrid, Spain (enrolling)
• Hospital Universitario Nuestra Señora de Candelaria — Santa Cruz de Tenerife, Spain (enrolling)
• Hospital General Universitario de Valencia — Valencia, Spain (enrolling)
• University Hospital Basel — Basel, Switzerland (enrolling)
• Kantonsspital Winterthur — Winterthur, Switzerland (enrolling)
• IRCCS - Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) — Meldola, Italy (enrolling)
• North Estonia Medical Centre Foundation — Talinn, Estonia (enrolling)
• Instituto Europeo di Oncologia (IEO) — Milan, Italy (enrolling)
• Ruhrlandklinik Essen — Essen, Germany (enrolling)
• Fondazione IRCCS Policlinico S. Matteo — Pavia, Italy (enrolling)
• Beaumont Hospital — Dublin, Ireland (enrolling)
• Nuovo Ospedale di Prato Santo Stefano — Prato, Italy (enrolling)
• St James's Hospital — Dublin, Ireland (enrolling)
• LMU München — München, Germany (enrolling)
• Azienda Ospedaliera Universitaria Integrata di Verona — Verona, Italy (enrolling)
• National University Hospital — Singapore, Singapore (enrolling)
• University of Perugia, AO SM Misericorida Perugia — Perugia, Italy
• CHU d'Angers — Angers, France

Full record on ClinicalTrials.gov

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