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NCT07489066 · ClinicalTrials.gov registry record · Phase 2

Symbiotic-Lung-10: A Study to Learn About PF-08634404 Alone or in Combination in Early-stage or Locally Advanced NSCLC

A Phase 2 study, sponsored by Pfizer.

Recruiting
Registry status
Phase 2
Development phase
120
Enrollment target

NCT07489066 is a Phase 2 study that is actively recruiting participants, run by Pfizer. The registered enrollment target is 120 participants.

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The verdict

NCT07489066, a Phase 2 study, is actively recruiting participants, sponsored by Pfizer.

RECRUITING
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

This study is being done to learn more about a new medicine called PF-08634404. The study team wants to understand how well it works when given alone or with chemotherapy. The study is for adults with early stage or locally advanced non-small cell lung cancer (NSCLC) that may or may not be removable with surgery. The study is seeking participants who: * Are aged 18 years or older * Have either: * Early-stage or locally advanced (Stage II or IIIA/B) NSCLC and are a candidate for neoadjuvant therapy, followed by surgical removal of the tumor. Neoadjuvant therapy is a treatment given as a first step to shrink the tumor before surgery. * Early-stage or locally advanced (Stage II or IIIA/B) NSCLC and are a candidate for adjuvant therapy and did not achieve a pathological complete response (pCR) from approved treatment that was administered before surgery. Adjuvant therapy is an additional cancer treatment given after the primary treatment to lower the risk that the cancer will come back. pCR is defined as absence of viable tumor in all surgically removed samples. * Locally advanced (Stage III) NSCLC that may not be removable with surgery, was treated with concurrent chemoradiotherapy (cCRT), and is a candidate for additional treatment, otherwise known as consolidation therapy. cCRT is chemotherapy and radiation given simultaneously. * Be in good physical condition and have healthy organs based on medical tests. * Do not have known actionable changes in DNA The study has 3 parts and each participant will be assigned to one part by their doctor based on their disease diagnosis: * Part A will test PF-08634404 given with chemotherapy in the neoadjuvant setting, followed by surgery. * Part B will test PF-08634404 alone in adults who already were treated with neoadjuvant chemo-immunotherapy, underwent surgery, and did not achieve pCR per tumor tissue pathology analysis. Neoadjuvant chemo-immunotherapy refers to the combination of chemotherapy with immunotherapy per

Interventions

  • BIOLOGICAL PF-08634404
  • DRUG Chemotherapy Regimen 1
  • DRUG Chemotherapy Regimen 2

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2026-06-01
Est. Completion 2031-07-30
Phase Phase 2

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT07489066

The ClinicalTrials.gov registry entry for NCT07489066 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which PF-08634404 is the first listed.

NCT07489066 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07489066 about?

NCT07489066 is a clinical study titled "Symbiotic-Lung-10: A Study to Learn About PF-08634404 Alone or in Combination in Early-stage or Locally Advanced NSCLC". This study is being done to learn more about a new medicine called PF-08634404. The study team wants to understand how well it works when given alone or with chemotherapy. The study is for adults with early stage or locally advanced non-small cell lung cancer (NSCLC) that may or may not be removable...

What is the current status of trial NCT07489066?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2026-06-01. Estimated completion is 2031-07-30.

What interventions are being tested in trial NCT07489066?

The interventions under investigation include: PF-08634404 (BIOLOGICAL), Chemotherapy Regimen 1 (DRUG), Chemotherapy Regimen 2 (DRUG).

Who is sponsoring clinical trial NCT07489066?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.