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NCT06012435 · ClinicalTrials.gov registry record · Phase 3
A Study of SGN-B6A Versus Docetaxel in Previously Treated Non-small Cell Lung Cancer
A Phase 3 study of Carcinoma, Non-Small Cell Lung, sponsored by Seagen, a wholly owned subsidiary of Pfizer.
- Active
- Registry status
- Phase 3
- Development phase
- 703
- Enrollment target
- 20
- Study locations
NCT06012435 is a Phase 3 study of Carcinoma, Non-Small Cell Lung that is active but no longer recruiting, run by Seagen, a wholly owned subsidiary of Pfizer. The registered enrollment target is 703 participants, above the 318-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (121% higher). The trial reports 20 study locations across 3 states.
The verdict
NCT06012435, a Phase 3 study of Carcinoma, Non-Small Cell Lung, is active but no longer recruiting, sponsored by Seagen, a wholly owned subsidiary of Pfizer.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 3
- Development phase
- 703 participants
- Enrollment target
- 20
- Study locations
Study Summary
This clinical trial is studying nonsquamous non-small cell lung cancer (NSCLC). Participants in this study must have cancer that has spread through their body or can't be removed with surgery. Participants in this study must have been treated with no more than a platinum-based chemotherapy and an anti-PD-(L)1 drug. Participants with tumors that have certain treatable genomic alterations must have had at least 1 drug for that genomic alteration, in addition to platinum-based chemotherapy. This clinical trial uses an experimental drug called sigvotatug vedotin, which is a type of antibody drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. This clinical trial also uses a drug called docetaxel. Docetaxel is an anticancer drug that has been approved to treat non-small cell lung cancer. It is usually given to patients who previously received another anticancer treatment. In this study, one group of participants will get sigvotatug vedotin on Days 1 and 15 during each 28-day-cycle. A second group of participants will get docetaxel on Day 1 during each 21-day cycle. This study is being done to see if sigvotatug vedotin works better than docetaxel to treat participants with NSCLC. This study will also test what side effects happen when participants take these drugs. A side effect is anything a drug does to the body besides treating the disease.
Conditions Studied
Interventions
- DRUG sigvotatug vedotin
- DRUG docetaxel
Study Locations (20)
California
- Providence Medical Foundation - Fullerton
- Providence St. Jude Medical Center Virginia K. Crosson Cancer Center and Infusion Center - Fullerton
- Providence St. Jude Medical Center - Fullerton
- Cancer and Blood Specialty Clinic - Los Alamitos
- Cancer Blood and Specialty Clinic - Los Alamitos
- Regulatory Management Only: TRIO-US Central Administration - Los Angeles
- Drug Management Only: UCLA West Medical Pharmacy Attn: Steven L. Wong, Pharma.D. - Los Angeles
- Drug Management Only: UCLA West Medical Pharmacy, Attn: Steven L Wong, Pharm.D. - Los Angeles
- UCSF Medical Center - Mission Bay - San Francisco
- Sansum Clinic - Santa Barbara
- Sansum Clinic - Solvang
Colorado
- Rocky Mountain Cancer Centers LLP - Aurora
- Rocky Mountain Cancer Centers LLP - Boulder
- Rocky Mountain Cancer Centers LLP - Colorado Springs
- Rocky Mountain Cancer Centers LLP - Colorado Springs
- Rocky Mountain Cancer Centers LLP - Denver
- Rocky Mountain Cancer Centers LLP - Denver
- Rocky Mountain Cancer Centers LLP - Lakewood
- Rocky Mountain Cancer Centers LLP - Littleton
Alaska
- Alaska Oncology and Hematology, LLC - Anchorage
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 703 participants |
| Start Date | 2024-02-21 |
| Est. Completion | 2028-03-11 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06012435
The ClinicalTrials.gov registry entry for NCT06012435 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 703 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 318-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (121% higher). The listed sponsor is Seagen, a wholly owned subsidiary of Pfizer, which has 28 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Carcinoma, Non-Small Cell Lung appearing as the primary indexed condition, and to 2 interventions - of which sigvotatug vedotin is the first listed.
NCT06012435 reports 20 study locations spanning 3 distinct geographic areas - top geographies include California, Colorado, Alaska.
Frequently Asked Questions
What is clinical trial NCT06012435 about?
NCT06012435 is a clinical study titled "A Study of SGN-B6A Versus Docetaxel in Previously Treated Non-small Cell Lung Cancer". This clinical trial is studying nonsquamous non-small cell lung cancer (NSCLC). Participants in this study must have cancer that has spread through their body or can't be removed with surgery. Participants in this study must have been treated with no more than a platinum-based chemotherapy and an an...
What is the current status of trial NCT06012435?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 703 participants. The study started on 2024-02-21. Estimated completion is 2028-03-11.
What conditions does trial NCT06012435 study?
This clinical trial studies the following conditions: Carcinoma, Non-Small Cell Lung.
What interventions are being tested in trial NCT06012435?
The interventions under investigation include: sigvotatug vedotin (DRUG), docetaxel (DRUG).
Who is sponsoring clinical trial NCT06012435?
This trial is sponsored by Seagen, a wholly owned subsidiary of Pfizer, which has 28 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06012435 being conducted?
This trial has 20 study locations across Alaska, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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