Trial · NCT03096275
Comparison of Mycophenolate Mofetil and Cyclophosphamide for Active Takayasu's Arteritis
NCT03096275, Phase 3, Completed, Chinese SLE Treatment And Research Group
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Mycophenolate Mofetil and Cyclophosphamide for Active Takayasu's Arteritis. Trials, record NCT03096275. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03096275
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Mycophenolate Mofetil and Cyclophosphamide for Active Takayasu's Arteritis
- NCT number
- NCT03096275
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 138 participants, actual
- Lead sponsor
- Chinese SLE Treatment And Research Group
- Conditions
- Takayasu Arteritis
- Interventions
- MMF, CYC, Glucocorticoids, MTX, AZA
- First posted
- 2017-03-30
- Last updated
- 2023-08-30
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Proportion of patients with complete remission | 52 weeks | The proportion of patients who reached the pre-defined criteria of complete remission in both groups |
| Secondary | Proportion of patients with partial remission | 52 weeks | Proportion of patients who reached the pre-defined partial remission criteria of the disease |
| Secondary | Safety profile of MMF combined with MTX | 52 weeks | Proportion of adverse events in both treatment groups |
| Secondary | Rate of complications | 52 weeks | Proportion of patients with complications in both treatment group |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers6
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03096275
GET https://conductscience.org/api/trials/v1/NCT03096275/registered