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Trial · NCT02228590

Results by group55

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

OutcomeGroupCategoryValueSpreadUnits
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-130277Overall78.9percentage of participants
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-13027715 minutes post-dose31.6percentage of participants
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-13027730 minutes post-dose78.9percentage of participants
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-13027745 minutes post-dose68.4percentage of participants
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-13027760 minutes post-dose68.4percentage of participants
The Percentage of Patients With Resolution of an 'OFF' Episode to an 'ON' State Following Administration of APL-130277APL-13027790 minutes post-dose47.4percentage of participants
Time to 'ON' State From Time of Dosing of APL-130277APL-13027724.0Standard Deviation 7.61minutes
Duration of 'ON' Response From Time of Dosing of APL-130277APL-13027750.0Standard Deviation 19.36minutes
Percentage of Patients Who Completed the Trial and Experienced an 'ON' EpisodeAPL-13027778.9percentage of participants
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027710 mg APL-130277 Dose 1 Day 12.01Standard Deviation 0.914ng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027715 mg APL-130277 Dose 2 Day 12.52Standard Deviation 1.04ng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027710 mg APL-130277 Dose 1 Day 24.18Standard Deviation NAng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027720 mg APL-130277 Dose 1 Day 23.82Standard Deviation 1.81ng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027725 mg APL-130277 Dose 2 Day 24.84Standard Deviation NAng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027720 mg APL-130277 Dose 1 Day 32.82Standard Deviation 1.38ng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027725 mg APL-130277 Dose 1 Day 312.3Standard Deviation NAng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027730 mg APL-130277 Dose 1 Day 34.22Standard Deviation NAng/mL
Pharmacokinetic (PK) Evaluation: Maximum Observed Plasma Concentration (Cmax)APL-13027725 mg APL-130277 Dose 2 Day 34.84Standard Deviation 2.99ng/mL
PK Evaluation: Time of Maximum Observed Plasma Concentration (Tmax)APL-13027710 mg APL-130277 Dose 1 Day 160.0Full Range 45.0 to 90.0minutes
PK Evaluation: Time of Maximum Observed Plasma Concentration (Tmax)APL-13027715 mg APL-130277 Dose 2 Day 135.0Full Range 24.0 to 90.0minutes

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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