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ACTIVE NOT RECRUITING Phase 3

A Study to Compare ABP 234 and Keytruda® (Pembrolizumab) in Participants With Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer

NCT06311721 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to compare the efficacy of ABP 234 with the pembrolizumab reference product (Keytruda®).

Interventions

  • DRUG ABP 234
  • DRUG Pembrolizumab (US)
  • DRUG Pembrolizumab (EU)

Study Locations (20)

California

  • Precision NextGen Oncology and Research Center — Beverly Hills
  • TOI Clinical Research — Cerritos
  • Cancer and Blood Specialty Clinic (CBSC) — Los Alamitos
  • Valkyrie Clinical Trials — Los Angeles
  • PIH Health Hospital — Whittier

Florida

  • Millennium Oncology - Hollywood — Hollywood
  • BRCR Medical Center Inc. — Tamarac

Texas

  • Millennium Research and Clinical Development, LLC — Houston
  • Texas Oncology, P.A — San Antonio

Buenos Aires

  • Instituto de Investigaciones Clinicas Mar del Plata — Mar del Plata
  • Centro de Investigacion Pergamino SA — Pergamino

Santa Fe Province

  • Sanatorio Britanico De Rosario — Rosario
  • Hospital Provincial del Centenario — Rosario

Illinois

  • Accellacare Duly — Plainfield

Iowa

  • Accellacare of McFarland — Ames

Michigan

  • Detroit Clinical Research Center, PC — Farmington Hills

Trial Details

FieldValue
Enrollment Target 315 participants
Start Date 2024-09-09
Est. Completion 2028-05-29
Phase Phase 3

Sponsor

Amgen

266 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06311721

The ClinicalTrials.gov registry entry for NCT06311721 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 315 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer appearing as the primary indexed condition, and to 3 interventions — of which ABP 234 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06311721 reports 20 study locations spanning 12 distinct geographic areas — top geographies include California, Florida, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06311721 about?

NCT06311721 is a clinical study titled "A Study to Compare ABP 234 and Keytruda® (Pembrolizumab) in Participants With Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer". The primary objective of this study is to compare the efficacy of ABP 234 with the pembrolizumab reference product (Keytruda®).

What is the current status of trial NCT06311721?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 315 participants. The study started on 2024-09-09. Estimated completion is 2028-05-29.

What conditions does trial NCT06311721 study?

This clinical trial studies the following conditions: Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06311721?

The interventions under investigation include: ABP 234 (DRUG), Pembrolizumab (US) (DRUG), Pembrolizumab (EU) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06311721?

This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06311721 being conducted?

This trial has 20 study locations across California, Florida, Illinois, Iowa, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial