OncoMatch

OncoMatch/Clinical Trials/NCT05061550

Neoadjuvant and Adjuvant Treatment in Resectable Non-small Cell Lung Cancer

Is NCT05061550 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments for non-small cell lung cancer.

Phase 2RecruitingAstraZenecaNCT05061550Data as of May 2026

Treatment: Durvalumab · Oleclumab · Monalizumab · Dato-DXd · AZD0171 · Carboplatin · Cisplatin · Pemetrexed/Cisplatin · Pemetrexed/Carboplatin · Carboplatin/Paclitaxel · Volrustomig · RilvegostomigThe study is intended to assess the safety and efficacy of perioperative treatment with Durvalumab in combination with Oleclumab, Monalizumab, or AZD0171 and platinum doublet chemotherapy (CTX); or Volrustomig or Rilvegostomig in combination with CTX; or Datopotamab deruxtecan (Dato-DXd) in combination with Durvalumab or Rilvegostomig and single agent platinum chemotherapy in participants with resectable, early-stage non-small cell lung cancer.

Check if I qualify

Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Excluded: EGFR sensitizing mutation

Participants with sensitising EGFR mutations

Excluded: ALK translocation

Participants with ... ALK translocations

Excluded: PD-L1 (CD274) expression <1%

Participants with baseline PD-L1 expression status <1% (Arms 6 and 7 only)

Disease stage

Required: Stage IIA, IIB, IIIA, IIIB

Performance status

WHO OR ECOG 0–1

Prior therapy

Cannot have received: immune-mediated therapy (anti-CTLA-4, anti-TIGIT, anti-PD-1, anti-PD-L1, anti-PD-L2, agents targeting the adenosine pathway, anti-NKG2A, anti-HLA-E agents, anti-LIF agents, TROP2 targeting ADC, ADC containing a chemotherapy agent that inhibits TOP1 activity)

Prior exposure to approved or investigational immune-mediated therapy including, but not limited to, other anti-CTLA-4, anti-TIGIT (T cell immunoreceptor with Ig and ITIM domains), anti-PD-1, anti-PD-L1, and anti-PD-L2 antibodies. Participants who received agents targeting the adenosine pathway, anti-NKG2A, anti-HLA-E agents, and anti-LIF agents are also excluded. Participants who have received previous treatment with a TROP2 targeting ADC or with another ADC containing a chemotherapy agent that inhibits TOP1 activity are also excluded.

Cannot have received: preoperative radiotherapy

Participants who have preoperative radiotherapy treatment as part of their care plan

Cannot have received: concurrent chemotherapy, investigational product, biologic, or hormonal therapy for cancer treatment

Any concurrent chemotherapy, investigational product, biologic, or hormonal therapy for cancer treatment

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ and bone marrow function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Research Site · Little Rock, Arkansas
  • Research Site · Los Angeles, California
  • Research Site · Oakland, California
  • Research Site · New Haven, Connecticut
  • Research Site · Stuart, Florida

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify