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Alkylating agents

Pembrolizumab for Non-Small Cell Lung Cancer

Phase 1
Waitlist Available
Research Sponsored by Nathan Pennell, MD, PhD
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Study Summary

This trial will test the safety of giving chemoradiotherapy followed by consolidation pembrolizumab after surgery in people with NSCLC.

Eligible Conditions
  • Non-Small Cell Lung Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of patients with grade 3 pulmonary toxicity or grade 4 other non hematologic toxicity
Secondary outcome measures
Complete Pathologic Response Rate
Nodal Downstaging at Surgery
Objective Response Rate
+2 more

Side effects data

From 2024 Phase 2 trial • 57 Patients • NCT03004183
21%
Fatigue
13%
Nausea
11%
Back pain
9%
Shortness of Breath
9%
Anemia
9%
Abdominal pain
9%
Diarrhea
7%
Pneumonia
7%
Kidney Injury and/or Infection
7%
Dyspnea
7%
Weight Loss
5%
Malnutrition, Hypercalcemia and Weakness
5%
Pneumothorax
5%
Intractable pain, back pain, hip pain
5%
Activated partial thromboplastin time prolonged
4%
Pleural effusion
4%
Atrial fibrillation with rapid ventricular response
2%
Thrombocytopenia
2%
Respiratory failure
2%
Skin rash
2%
colitis
100%
80%
60%
40%
20%
0%
Study treatment Arm
Single Arm

Trial Design

1Treatment groups
Experimental Treatment
Group I: Resectable PatientsExperimental Treatment4 Interventions
Chemoradiation (Cisplatin + Etoposide + Pembrolizumab with concurrent radiation). Patients will be assessed for surgery followed by consolidation therapy
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Etoposide
FDA approved
Pembrolizumab
FDA approved
Radiation
2003
Completed Phase 3
~1020
Cisplatin
FDA approved

Find a Location

Who is running the clinical trial?

Nathan Pennell, MD, PhDLead Sponsor
2 Previous Clinical Trials
45 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this study actively seeking participants?

"This study is currently not open for recruitment. It was initially published on May 19th 2017 and last modified August 19th, 2022. If you are searching for alternative trials, there are 1909 lung cancer studies and 1764 Pembrolizumab clinical trials actively recruiting participants."

Answered by AI

What maladies does Pembrolizumab typically address?

"Pembrolizumab is commonly employed to treat malignant melanoma of the skin, but also proves effective in treating merkel cell cancer, recurrent cervical neoplasms and refractory/relapsed mediastinal large B-cell lymphoma."

Answered by AI

What is the total enrolment for this research initiative?

"Presently, this medical trial is not taking any more patients. Initially posted on May 19th 2017 and updated lastly on August 19th 2022, it no longer seeks to enrol participants. However those looking for other studies may find 1909 studies recruiting lung cancer sufferers and 1764 seeking Pembrolizumab users respectively."

Answered by AI

Is there any risk associated with administering Pembrolizumab to patients?

"The safety of Pembrolizumab has been determined to be a 1 on the scale from 1-3, as this trial is in its initial phase with limited evidence for both efficacy and security."

Answered by AI

What have prior investigations elucidated about Pembrolizumab?

"Presently, 405 Phase 3 clinical trials for Pembrolizumab are underway with the majority situated in Shanghai. Simultaneously, there are 1764 active studies of this drug being conducted across 77,414 locations around the world."

Answered by AI
~1 spots leftby Apr 2025