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Disease · MONDO_0006451

Comparisons in its trials11

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Treatment: Weeks 1-4, Group 1; Weeks 1-2, Group 2 vs No Treatment: Weeks 5-6, Group 1; Week 3, Group 2: Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0).
41 of 4115 of 1556NCT01621568Trial comparisons
Treatment: Weeks 1-4, Group 1; Weeks 1-2, Group 2 vs No Treatment: Weeks 5-6, Group 1; Week 3, Group 2: deaths from any cause38 of 4115 of 1556NCT01621568Trial comparisons
Treatment: Weeks 1-4, Group 1; Weeks 1-2, Group 2 vs No Treatment: Weeks 5-6, Group 1; Week 3, Group 2: serious adverse events38 of 4115 of 1556NCT01621568Trial comparisons
Thymoma vs Thymic Carcinoma: serious adverse events13 of 2414 of 2145NCT00010257Trial comparisons
Thymoma Patients vs Thymic Patients: Number of Participants With a Partial Response2 of 250 of 1641NCT00589290Trial comparisons
Thymoma vs Thymic Carcinoma: Grade 3/4 Treatment Related Adverse Events1 of 161 of 1127NCT00198133Trial comparisons
Thymoma vs Thymic Carcinoma: serious adverse events2 of 163 of 1127NCT00198133Trial comparisons
Thymoma vs Thymic Carcinoma: Expected Toxicities Including Skin Rashes and Diarrhea10 of 123 of 921NCT00718809Trial comparisons
Thymoma vs Thymic Carcinoma: serious adverse events2 of 121 of 921NCT00718809Trial comparisons
Experimental: Arm A (Ramucirumab, Carboplatin, Paclitaxel) vs Active Comparator: Arm B (Carboplatin, Paclitaxel): deaths from any cause1 of 82 of 917NCT03694002Trial comparisons
Experimental: Arm A (Ramucirumab, Carboplatin, Paclitaxel) vs Active Comparator: Arm B (Carboplatin, Paclitaxel): serious adverse events3 of 80 of 917NCT03694002Trial comparisons

diseases-2026-09-18-0.1.0

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
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
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

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/diseases/v1/MONDO_0006451/comparisons