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Disease · MONDO_0015759

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
Group B (Chemotherapy, Protective Therapy, Monoclonal Antib.) vs Group C (Chemotherapy, Monoclonal Antibody Therapy): serious adverse events2 of 466 of 4288NCT00057811Trial comparisons
Part A: PS-341 Alone vs Part B: PS-341 & EPOCH: serious adverse events21 of 2440 of 4468NCT00054665Trial comparisons
Part A: PS-341 Alone vs Part B: PS-341 & EPOCH: Number of Participants With Adverse Events23 of 2344 of 4467NCT00054665Trial comparisons
R-HCVAD/MA vs R-CHOP: Progression Free Survival (Rate)35 of 497 of 1059NCT00290498Trial comparisons
RHCVAD vs RCHOP: deaths from any cause4 of 490 of 1059NCT00290498Trial comparisons
RHCVAD vs RCHOP: serious adverse events49 of 497 of 1059NCT00290498Trial comparisons
Phase I: Induction vs Phase II: Maintenance: serious adverse events3 of 191 of 2948NCT00634179Trial comparisons
Fenretinide and Rituximab (Rituximab Naive) vs Fenretinide and Rituximab (Rituximab Pre Treated): Response Rates of B-Non-Hodgkin Lymphoma to the Combination of Rituximab and Fenretinide (Phase II)4 of 70 of 1623NCT00288067Trial comparisons
MEDI-551 12 mg/kg and MEDI0680 2.5 mg/kg vs MEDI-551 12 mg/kg and MEDI0680 10 mg/kg: Number of Participants With Positive Anti-Drug Antibodies (ADA) for MEDI-551 and MEDI06801 of 50 of 510NCT02271945Trial comparisons
MEDI-551 12 mg/kg and MEDI0680 2.5 mg/kg vs MEDI-551 12 mg/kg and MEDI0680 10 mg/kg: deaths from any cause3 of 53 of 510NCT02271945Trial comparisons
MEDI-551 12 mg/kg and MEDI0680 2.5 mg/kg vs MEDI-551 12 mg/kg and MEDI0680 10 mg/kg: serious adverse events2 of 51 of 510NCT02271945Trial 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_0015759/comparisons