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Disease · MONDO_0044889

Comparisons in its trials13

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
Arm A: Mosun-Pola vs Arm B: R-GemOx: deaths from any cause66 of 13535 of 64199NCT05171647Trial comparisons
Arm A: Mosun-Pola vs Arm B: R-GemOx: serious adverse events45 of 13516 of 64199NCT05171647Trial comparisons
Cohort A: Loncastuximab Tesirine + Rituximab (Lonca-R) vs Cohort B: Loncastuximab Tesirine + Rituximab (Lonca-R): Number of Participants With Confirmed Positive Anti-Drug Antibody (ADA) Response0 of 170 of 2441NCT05144009Trial comparisons
Cohort A: Loncastuximab Tesirine + Rituximab (Lonca-R) vs Cohort B: Loncastuximab Tesirine + Rituximab (Lonca-R): deaths from any cause5 of 1710 of 2441NCT05144009Trial comparisons
Cohort A: Loncastuximab Tesirine + Rituximab (Lonca-R) vs Cohort B: Loncastuximab Tesirine + Rituximab (Lonca-R): serious adverse events13 of 1716 of 2441NCT05144009Trial comparisons
Arm A: Glofit-GemOx vs Arm B: Mosun-GemOx: Number of Deaths Due to Adverse Events (AEs)1 of 170 of 623NCT04313608Trial comparisons
Arm A: Glofit-GemOx vs Arm B: Mosun-GemOx: Number of Treatment Discontinuations Due to AE1 of 171 of 623NCT04313608Trial comparisons
Arm A: Glofit-GemOx vs Arm B: Mosun-GemOx: deaths from any cause1 of 170 of 623NCT04313608Trial comparisons
Arm A: Glofit-GemOx vs Arm B: Mosun-GemOx: serious adverse events12 of 174 of 623NCT04313608Trial comparisons
Dose Escalation: Arm 1, Dose Level 1, Original: 30mg Copanlisib vs Dose Escalation: Arm 1, Dose Level 1, Modified: 30mg Copanlisib: Number of Participants With Dose Limiting-toxicity (DLT)2 of 51 of 38NCT04933617Trial comparisons
Dose Escalation: Arm 1, Dose Level 1, Original: 30mg Copanlisib vs Dose Escalation: Arm 1, Dose Level 1, Modified: 30mg Copanlisib: Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)
5 of 53 of 38NCT04933617Trial comparisons
Dose Escalation: Arm 1, Dose Level 1, Original: 30mg Copanlisib vs Dose Escalation: Arm 1, Dose Level 1, Modified: 30mg Copanlisib: deaths from any cause5 of 50 of 38NCT04933617Trial comparisons
Dose Escalation: Arm 1, Dose Level 1, Original: 30mg Copanlisib vs Dose Escalation: Arm 1, Dose Level 1, Modified: 30mg Copanlisib: serious adverse events2 of 50 of 38NCT04933617Trial 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.

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