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Recruiting Phase 1 NCT02889666

NCT02889666 A Randomised Trial of Chemotherapy Plus Surgery for Recurrent Non-Small Cell Lung Cancer

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Clinical Trial Summary
NCT ID NCT02889666
Status Recruiting
Phase Phase 1
Sponsor Shanghai Jiao Tong University School of Medicine
Condition Recurrent Non-small Cell Lung Cancer
Study Type INTERVENTIONAL
Enrollment 500 participants
Start Date 2008-01
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
CisplatinCarboplatinDocetaxel

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 500 participants in total. It began in 2008-01 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to determine if the commonly administered chemotherapeutic agents including cisplatin, carboplatin, oxaliplatin, docetaxel and gemcitabine for solid tumors in clinical oncology, either a single format or given as combinations followed by surgery are effective in the treatment of relapsed and refractory non-small cell lung cancer patients.

Eligibility Criteria

Inclusion Criteria: * Age ≤ 75 years with histologically proven NSCLC * No severe major organ dysfunction * WHO performance status of 0 or 1 * No prior cancer chemotherapy * A Clinical Stage ≥ IA (T1a, N0, M0) of lung disease but without diagnosed distant metastasis (according to the 1997 revision of the International Union Against Cancer TNM staging system) as determined by a preoperative evaluation that included a pleural computed tomography (CT) scan. Exclusion Criteria: * Age ≥ 76 * Severe major organ dysfunction * WHO performance status of \>1 * Prior cancer chemotherapy * Stage IV

Contact & Investigator

Central Contact

Yu Sun, Ph.D

✉ sunyu@sibs.ac.cn

📞 86-21-54923302

Principal Investigator

Yu Sun, Ph.D

PRINCIPAL INVESTIGATOR

Shanghai Jiao Tong University School of Medicine

Frequently Asked Questions

Who can join the NCT02889666 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Recurrent Non-small Cell Lung Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT02889666 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT02889666 currently recruiting?

Yes, NCT02889666 is actively recruiting participants. Contact the research team at sunyu@sibs.ac.cn for enrollment information.

Where is the NCT02889666 trial being conducted?

This trial is being conducted at Changchun, China, Shanghai, China, Shanghai, China.

Who is sponsoring the NCT02889666 clinical trial?

NCT02889666 is sponsored by Shanghai Jiao Tong University School of Medicine. The principal investigator is Yu Sun, Ph.D at Shanghai Jiao Tong University School of Medicine. The trial plans to enroll 500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology