Trial · NCT03106779
Outcomes15
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 15 of 15
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Major Molecular Response (MMR) Rate at 24 Weeks | 24 weeks | Full Analysis Set (FAS): The FAS comprised of all randomized patients. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Number of Participants With Major Molecular Response (MMR) Rate | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Complete Cytogenetic Response Rate | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Time to MMR | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Duration of MMR | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Time to CCyR | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Duration of CCyR | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Time to Treatment Failure | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Progression Free Survival | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Overall Survival | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | Trough Plasma Concentrations | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | PK Parameter: Cmax, | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | PK Parameter: Tmax | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | PK Parameter: AUC0-12h | 96 weeks after the last patient received the first study dose | |||
| SECONDARY | PK Parameter: CL/F | 96 weeks after the last patient received the first study dose |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT03106779/outcomes