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

NCT05061550 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 630

Last updated 2026-05-22

No results posted yet for this study

Summary

The 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.

Conditions

Interventions

DRUG

Durvalumab

Participants will receive Durvalumab via intravenous route.

DRUG

Oleclumab

Participants will receive Oleclumab via intravenous route.

DRUG

Monalizumab

Participants will receive Monalizumab via intravenous route.

DRUG

Dato-DXd

Participants will receive datopotamab deruxtecan (Dato-DXd) via intravenous route.

DRUG

AZD0171

Participants will receive AZD0171 via intravenous route.

DRUG

Carboplatin

Carboplatin as chemotherapy

DRUG

Cisplatin

Cisplatin as chemotherapy

DRUG

Pemetrexed/Cisplatin

Pemetrexed/Cisplatin as chemotherapy

DRUG

Pemetrexed/Carboplatin

Pemetrexed/Carboplatin as chemotherapy

DRUG

Carboplatin/Paclitaxel

Carboplatin/Paclitaxel, as chemotherapy

DRUG

Volrustomig

Participants will receive Volrustomig via intravenous route.

DRUG

Rilvegostomig

Participants will receive Rilvegostomig via intravenous route.

Sponsors & Collaborators

  • Parexel

    collaborator INDUSTRY
  • AstraZeneca

    lead INDUSTRY

Principal Investigators

  • Tina Cascone, MD · MD Anderson Cancer Center Houston, TX 77030

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-14
Primary Completion
2030-05-28
Completion
2030-05-28
FDA Drug
Yes

Countries

  • United States
  • Belgium
  • Canada
  • France
  • Hungary
  • Ireland
  • Italy
  • Portugal
  • South Korea
  • Spain
  • Taiwan
  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05061550 on ClinicalTrials.gov