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Trial · NCT01235741

Results by group49

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

OutcomeGroupCategoryValueSpreadUnits
Percent Change From Baseline to Week 1 and From Baseline to Month 6 Follow-up in Body Weight - Intent to Treat PopulationPlaceboWeek 1-0.34Standard Deviation 0.924percentage of change in weight
Percent Change From Baseline to Week 1 and From Baseline to Month 6 Follow-up in Body Weight - Intent to Treat PopulationPramlintide + MetreleptinWeek 1-0.26Standard Deviation 0.819percentage of change in weight
Percent Change From Baseline to Week 1 and From Baseline to Month 6 Follow-up in Body Weight - Intent to Treat PopulationPlacebo6 Month Follow-Up-0.02Standard Deviation 6.575percentage of change in weight
Percent Change From Baseline to Week 1 and From Baseline to Month 6 Follow-up in Body Weight - Intent to Treat PopulationPramlintide + Metreleptin6 Month Follow-Up-1.80Standard Deviation 6.063percentage of change in weight
Number of Participants With Treatment Emergent Adverse Events and Number With Post Treatment Adverse Events - Intent to Treat PopulationOn Treatment Placebo6participants
Number of Participants With Treatment Emergent Adverse Events and Number With Post Treatment Adverse Events - Intent to Treat PopulationOn Treatment Pramlintide + Metreleptin13participants
Number of Participants With Treatment Emergent Adverse Events and Number With Post Treatment Adverse Events - Intent to Treat PopulationPost Treatment Placebo Arm13participants
Number of Participants With Treatment Emergent Adverse Events and Number With Post Treatment Adverse Events - Intent to Treat PopulationPost Treatment Pramlintide + Metreleptin Arm16participants
Change From Baseline to Week 2, and to Follow up Months 2, 4, 6 in Fasting Leptin Concentration - Intent to Treat PopulationPramlintide + MetreleptinChange from baseline to Week 2 of treatment223.38Standard Deviation 512.088ng/mL
Change From Baseline to Week 2, and to Follow up Months 2, 4, 6 in Fasting Leptin Concentration - Intent to Treat PopulationPramlintide + MetreleptinChange from baseline to Month 2 Follow up15.46Standard Deviation 34.885ng/mL
Change From Baseline to Week 2, and to Follow up Months 2, 4, 6 in Fasting Leptin Concentration - Intent to Treat PopulationPramlintide + MetreleptinChange from baseline to Month 4 Follow up20.08Standard Deviation 35.732ng/mL
Change From Baseline to Week 2, and to Follow up Months 2, 4, 6 in Fasting Leptin Concentration - Intent to Treat PopulationPramlintide + MetreleptinMonth 6 Follow up10.70Standard Deviation 18.913ng/mL
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinWeek 10participants
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinWeek 21participants
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinEarly Termination9participants
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinMonth 2 Follow-Up15participants
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinMonth 4 Follow-Up10participants
Number of Participants With Anti-leptin Antibodies Who Received Metreleptin - Intent to Treat PopulationPramlintide + MetreleptinMonth 6 Follow-Up8participants
Number of Participants With Neutralizing Activity to Metreleptin at Early Termination or During Post Treatment Follow-Up - Intent to Treat Population Who Received MetreleptinPramlintide + Metreleptin0participants
Number of Participants With Hematology and Urinalysis Laboratory Values of Potential Clinical Importance - Intent to Treat PopulationPlaceboHematocrit0participants

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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