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Trial · NCT03770000

Results by group22

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 1No.of Participants with Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 2No.of Participants with Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 3No.of Participants with Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose expansion_Group 1 (PTCL)No.of Participants with Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose expansion_Group 2 (CTCL)No.of Participants with Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 1No.of Participants without Dose Limiting Toxicities3Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 2No.of Participants without Dose Limiting Toxicities3Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose escalation_Cohort 3No.of Participants without Dose Limiting Toxicities3Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose expansion_Group 1 (PTCL)No.of Participants without Dose Limiting Toxicities0Participants
Number of Participants With and Without Dose Limiting Toxicities (DLTs)Dose expansion_Group 2 (CTCL)No.of Participants without Dose Limiting Toxicities0Participants
Overall Response Rate (ORR) With Tenalisib and Romidepsin CombinationDose escalation_Cohort 12Participants
Overall Response Rate (ORR) With Tenalisib and Romidepsin CombinationDose escalation_Cohort 22Participants
Overall Response Rate (ORR) With Tenalisib and Romidepsin CombinationDose escalation_Cohort 30Participants
Overall Response Rate (ORR) With Tenalisib and Romidepsin CombinationDose expansion_Group 1 (PTCL)7Participants
Overall Response Rate (ORR) With Tenalisib and Romidepsin CombinationDose expansion_Group 2 (CTCL)6Participants
Duration of Response (DoR) With Tenalisib and Romidepsin CombinationDose escalation_Cohort 115195% Confidence Interval 65 to 151days
Duration of Response (DoR) With Tenalisib and Romidepsin CombinationDose escalation_Cohort 215195% Confidence Interval 65 to 151days
Duration of Response (DoR) With Tenalisib and Romidepsin CombinationDose expansion_Group1 (PTCL Patients)15195% Confidence Interval 65 to 151days
Duration of Response (DoR) With Tenalisib and Romidepsin CombinationDose expansion_Group2 (CTCL Patients)11495% Confidence Interval 57 to 114days
Maximum Observed Plasma Concentration (Cmax)Dose escalation_Cohort 11544.42Standard Deviation 1609.44nanogram/millilitre

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.

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