RCTNCT00148486Phase 2 · 2003 · n=261 · Boehringer Ingelheim Parkinson Disease
tested Mean change from Baseline to Week 14 in the score of the UPDRS, Parts I-III combined
result Completed; results not posted
RCTNCT00148512Phase 2 · 2003 · n=254 · Boehringer Ingelheim Parkinson Disease
tested UPDRS parts II (averaged "on" and "off")
result Completed; results not posted
RCTNCT00153010Phase 2 · 2003 · n=430 · Boehringer Ingelheim Alzheimer Disease
tested Changes in Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog)
result Completed; results not posted
Obesity
tested Percent change and absolute change in body weight
result Completed; results not posted
Obesity
tested Effect on 24-h EE (energy expenditure) after 14 days dosing, adjusted for FFM(Fat-Free Mass) and FM (Fat Mass) changes
result Completed; results not posted
Type 2 Diabetes Mellitus
tested Effects of Co-administration of Tesofensine/Metoprolol Treatment vs. Placebo on 24-hour Mean Heart Rate
result −3.0 beats per minutes (BPM) (Effects of Co-administration of Tesofensine/Metopr…)
Confirmed Genetic Diagnosis of Prader-Willi Syndrome
tested Percent Change From Baseline to End of Treatment in Mean Body Weight
Small sample; effect at the edge of clinical significance.
Healthy Male Subjects
tested AUC0-48
Hypothalamic Injury-induced Obesity (HIO)
tested Number of Participants With Treatment Emergent Adverse Events
result +5.0 Participants (Number of Participants With Treatment Emergent Adv…)
Small sample; effect at the edge of clinical significance.
Treatment studies
tested cognitive subscale score
result Two 4‑week placebo‑controlled studies in 62 mild AD patients were modeled; the model correctly predicted the outcome of a subsequent 14‑week phase IIb trial in 430 patients that was negative.
Published human study (PubMed / Europe PMC), extracted from its abstract — not a CT.gov-registered trial.
OpenNCT00006077Phase 2 · 2000 · n=50 · National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease
result Completed; results not posted
OpenNCT00481104Phase 2 · 2007 · n=140 · NeuroSearch A/S Obesity
tested Safety measures: Treatment emergent adverse events, vital signs (BP and HR), ophthalmoscopy, ECG, laboratory assessments and physical examination
result Completed; results not posted
Non-randomised; effect size cannot be separated from placebo.
Preclinical / mechanistic research
tested rat · Sex-specific effects of appetite suppressants and stereotypy in rats
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Expression of brain derived neurotrophic factor, activity-regulated cytoskeleton protein mRNA, and enhancement of adult hippocampal neurogenesis in rats after sub-chronic and chronic treatment with the triple monoamine re-uptake inhibitor tesofensine.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Tesofensine, a novel triple monoamine reuptake inhibitor, induces appetite suppression by indirect stimulation of alpha1 adrenoceptor and dopamine D1 receptor pathways in the diet-induced obese rat.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · The novel triple monoamine reuptake inhibitor tesofensine induces sustained weight loss and improves glycemic control in the diet-induced obese rat: comparison to sibutramine and rimonabant.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Triple monoamine inhibitor tesofensine decreases food intake, body weight, and striatal dopamine D2/D3 receptor availability in diet-induced obese rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Anti-hypertensive treatment preserves appetite suppression while preventing cardiovascular adverse effects of tesofensine in rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Tesofensine induces appetite suppression and weight loss with reversal of low forebrain dopamine levels in the diet-induced obese rat.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.
Preclinical / mechanistic research
tested rat · Sex-specific effects of appetite suppressants on stereotypy in rats.
result Preclinical publication captured from PubMed/Europe PMC; effect details require paper-level extraction.