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NCT01124630 · ClinicalTrials.gov registry record · Phase 1
Study of CS-1008 in Combination With FOLFIRI in Patients Who Have Failed Other Treatments
A Phase 1 study, sponsored by Daiichi Sankyo.
- Completed
- Registry status
- Phase 1
- Development phase
- 21
- Enrollment target
NCT01124630: Completed Phase 1 study, sponsored by Daiichi Sankyo.
NCT01124630 is a Phase 1 study that has completed, run by Daiichi Sankyo. The registered enrollment target is 21 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01124630, a Phase 1 study, has completed, sponsored by Daiichi Sankyo.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 21 participants
- Enrollment target
Study Summary
Treatment with CS-1008 in combination with FOLFIRI (irinotecan, leucovorin, and 5-fluorouracil \[5-FU\]) in subjects with metastatic colorectal cancer (CRC) who have failed first-line treatment that was not irinotecan-based.
Primary Outcome
To obtain a preliminary assessment of the antitumor activity of CS-1008 in combination with a FOLFIRI regimen based on the Objective Response Rate (ORR)
Interventions
- DRUG FOLFIRI
- DRUG CS-1008
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2010-05 |
| Est. Completion | 2013-08 |
| Phase | Phase 1 |
What the finished NCT01124630 record still lists
NCT01124630 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower).
The record links to 0 conditions, and to 2 interventions - of which FOLFIRI is the first listed.
NCT01124630 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01124630 about?
NCT01124630 is a clinical study titled "Study of CS-1008 in Combination With FOLFIRI in Patients Who Have Failed Other Treatments". Treatment with CS-1008 in combination with FOLFIRI (irinotecan, leucovorin, and 5-fluorouracil \[5-FU\]) in subjects with metastatic colorectal cancer (CRC) who have failed first-line treatment that was not irinotecan-based.
What is the current status of trial NCT01124630?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2010-05. Estimated completion is 2013-08.
What interventions are being tested in trial NCT01124630?
The interventions under investigation include: FOLFIRI (DRUG), CS-1008 (DRUG).
Who is sponsoring clinical trial NCT01124630?
This trial is sponsored by Daiichi Sankyo, which has 236 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01124630's enrollment target sits among peer trials
21 1615th of 2000 higher than 372 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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