CompletedPhase 2NCT03794544
Official study title

Neoadjuvant Durvalumab Alone or in Combination With Novel Agents in Resectable Non-Small Cell Lung Cancer

Study summary

Study D9108C00002 (NeoCOAST) is a platform study assessing the effectiveness and safety of neoadjuvant durvalumab alone or in combination with novel agents in participants with resectable, early-stage (Stage I \[\>2cm\] to IIIA) non-small cell lung cancer (NSCLC).

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedDurvalumab and Oleclumab

Plus 2 other study approaches.

Who it may be forNon-small cell lung cancer (NSCLC) · Early-stage or resectable

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Feb 24, 2022 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 2

Interventional

Where is it offered?18 U.S. locations

Locations may change over time.

Who runs it?MedImmune LLC

Study sponsor

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Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 2
Sponsor
MedImmune LLC
Interventions being studied
Drug: Durvalumab; Combination Product: Oleclumab; Combination Product: Monalizumab; Combination Product: Danvatirsen
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

1. Cytologically and/or histologically-documented NSCLC 1. Stage I (\> 2 cm) to IIIA (for participants with N2 disease, only those with 1 single nodal station ≤ 3 cm are eligible) NSCLC according to the 8th edition of American Joint Committee on Cancer staging classification 2. Amenable to complete surgical resection 3. Have not received any other therapy for this condition 2. Predicted forced expiratory volume in one second (FEV1) ≥ 50% 3. Predicted diffusing capacity of the lungs for carbon monoxide (DLCO) ≥ 50% 4. ECOG 0 or 1 5. Adequate organ function

Reasons someone may not be able to joinExclusion criteria

1. Participants with small-cell lung cancer or mixed small-cell lung cancer 2. Participants who require or may require pneumonectomy 3. Prior treatment with programmed cell death ligand-1 (PD-L1), PD-L1, or cytotoxic T-lymphocyte antigen 4 (CTLA-4) inhibitors 4. Current or prior use of immunosuppressive medication within 14 days before the first dose of study drug. 5. Active or prior documented autoimmune or inflammatory disorders. The following are exceptions to this criterion: 1. Participants with vitiligo or alopecia 2. Participants with hypothyroidism on hormone replacement 3. Any chronic skin condition that does not require systemic therapy 4. Participants without active disease in the last 5 years may be included but only after consultation with the study physician 5. Participants with celiac disease controlled by diet alone 6. Pregnant or breast-feeding female 7. Major surgical procedure within prior 30 days 8. History of active primary immunodeficiency 9. Active infection including tuberculosis, hepatitis B, hepatitis C, or HIV 10. QTc interval (QTc) ≥ 470 ms 11. Uncontrolled intercurrent illness that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the participant to give written informed consent 12. Receipt of live attenuated vaccination within 30 days prior to study entry 13. History of another primary malignancy except for: 1. Curative-treated malignancy with no known active disease \> 2 years before enrollment on the study 2. Curative-treated non-melanoma skin cancer and/or carcinoma in-situ

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Research SiteLa Jolla, California
  • Research SiteFort Myers, Florida
  • Research SiteLeesburg, Florida
  • Research SiteBaltimore, Maryland
  • Research SiteBuffalo, New York
  • Research SiteNew York, New York
  • Research SiteChattanooga, Tennessee
  • Research SiteNashville, Tennessee
  • Research SiteHouston, Texas
  • Research SiteFairfax, Virginia
  • Research SiteMontreal, Quebec
  • Research SiteMarseille

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Feb 24, 2022. Always confirm current availability with the study team.

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