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NCT Number: NCT06246110

A Phase 2 Study of EIK1001 in Combo With Pembrolizumab and Chemotherapy in Patients With Stage 4 NSCLC

This study is for patients with advanced/metastatic non-small cells lung cancer (NSCLC) who have not received any treatment through the vein for the advanced disease.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Southern Cancer Care, Daphne, Alabama, United States

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About this study

This is a multicenter open-label phase 2 trial that aim to assess the safety, tolerability, and efficacy of EIK1001 in combination with standard of care in participants with both confirmed stage 4 squamous and non-squamous NSCLC who have not received prior systemic therapy for the advanced disease. The study includes dose finding and evaluates adverse events and efficacy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • be ≥ 18 years of age on the day of signing of informed consent.
  • confirmed Stage 4 NSCLC (squamous or non-squamous) and be considered for standard of care.
  • have confirmation that mutation-directed therapy is not indicated (documentation of absence of tumor activating mutations/fusions that are approved for first line therapy).
  • have at least 1 lesion with measurable disease at Baseline according to RECIST 1.1 as determined by the local site Investigator/radiology assessment.
  • have not received prior systemic treatment for advanced/metastatic NSCLC.
  • have an ECOG Performance Status of 0 to 1.
  • have adequate organ function.

Exclusion criteria

  • does not have predominantly squamous cell or non-squamous cell histology NSCLC. Mixed tumors will be categorized by the predominant cell type; if small cell elements are present, the participant is ineligible.
  • is currently participating in or has participated in a study of an investigational agent and received investigational therapy within 4 weeks or 5 half-lives (whichever is shorter) of administration of EIK1001.
  • prior to the first dose of EIK1001, has received prior systemic therapy for metastatic disease, or had major surgery (< 3 weeks prior to the first dose).
  • has completed palliative radiotherapy within 7 days of the first dose of study drug administration.
  • has a known history of prior malignancy, except if the participant has undergone potentially curative therapy with no evidence of that disease recurrence for 5 years.
  • has an active infection requiring therapy.

Treatment and study plan

EIK1001

Drug

EIK1001 is a Toll like receptor 7/8 (TLR 7/8) agonist

Pembrolizumab

Drug

PD-1 inhibitor

paclitaxel

Drug

Chemotherapy

Pemetrexed

Drug

Chemotherapy

carboplatin

Drug

Chemotherapy

Primary outcomes

  1. Percentage of participants with safety event during treatment

    Time frame: Up to 2 years

    Defined AEs that occur during treatment and are deemed to be related EIK1001 or combination with SOC or due to disease progression or toxicity.

Secondary outcomes

  1. Percentage of participants with objective response rate (ORR) and duration of response (DOR).

    Time frame: Up to 4 years

    Objective response (OR) is defined as participants who have a confirmed complete response (CR) or partial response (PR) by RECIST 1.1 and DOR is defined as the time from the first documented evidence of CR or PR until disease progression or death due to any cause, whichever occurs first, in participants demonstrating CR or PR, as assessed by the investigator.

Other outcomes

  1. Overall Survival (OS) at Final Follow-Up

    Time frame: Up to 4 years

    OS defined as the time from the first dose of study medication to death due to any cause

  2. Progression Free Survival (PFS)

    Time frame: Up to 4 years

    Progression-free survival (PFS) is defined as the time from the first dose of the study medication to the first documented disease progression by RECIST 1.1 (Investigator) or death due to any cause, whichever occurs first

Sponsors and collaborators

Lead sponsor

Eikon Therapeutics

Industry

Registry information

Official study title

A Phase 2 Study of EIK1001 in Combination With Pembrolizumab and Chemotherapy in Patients With Stage 4 Non-Small Cell Lung Cancer

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Feb 7, 2024
Registry last updated
May 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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