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Phase 2 N=30 Randomized Double-blind Treatment

Botulinum Toxin A to Treat Arm Tremor

Essential Tremor of the Upper Limbs

Enrolled (actual)
30
Serious AEs
6.7%
Results posted
Feb 2021
Primary outcome: Primary: Change From Baseline to Week 4 in Maximum Angular Tremor Amplitude of the Wrist (Injected Limb) — -0.47; 0.07 degree — p=0.144

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
IncobotulinumtoxinA (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Merz Pharmaceuticals GmbH
Primary completion
May 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline to Week 4 in Maximum Angular Tremor Amplitude of the Wrist (Injected Limb)
-0.47; 0.07 0.144
SECONDARY
Change From Baseline to Week 4 in Maximum Log-transformed Accelerometric Tremor Amplitude at Wrist Level (Injected Limb)
-0.73; 0.05
SECONDARY
Change From Baseline to Week 4 in Fahn-Tolosa-Marin (FTM) Tremor Score in Injected Limb (Item 5 [Right Upper Extremity] or 6 [Left Upper Extremity])
-1.9; -0.5
SECONDARY
Change From Baseline to Week 4 in FTM Motor Performance Score (Items 11-15)
-2.8; -0.8
SECONDARY
Participant's Global Impression of Change Scale (GICS) at Week 4
0.6; 0.3
SECONDARY
Investigator's Global Impression of Change Scale (GICS) at Week 4
0.8; 0.1

Summary

The objective of this study is to assess the efficacy and safety of a single, kinematic-analysis-based intramuscular injection of NT 201, compared with placebo, in moderate to marked essential tremor of the upper limb.

Eligibility Criteria

Main Inclusion Criteria:

  • Diagnosis of 'definite essential tremor' in accordance with modified TRIG criteria, as follows:
  • Bilateral postural tremor with or without kinetic tremor, involving hands and forearms, that is visible and persistent.
  • It is to be noted that:
  • Tremor of other body parts may be present in addition to upper limb tremor.
  • Bilateral tremor may be asymmetric.
  • Tremor is reported by patient to be persistent, although the amplitude may fluctuate.
  • First onset of essential tremor at least 6 months before screening with stability of the tremor symptoms over 4 weeks and in the opinion of the investigator definite diagnosis of essential tremor.
  • Moderate-to-marked upper-limb postural and/or kinetic tremor at wrist level, corresponding to Fahn-Tolosa-Marin upper-limb tremor rating of at least 2 categories (scale part C, items 16-23) in the limb to be treated between of 2 or higher.
  • Visible tremor at wrist level in at least one of the four positions/tasks used in kinematic assessments
  • Tremor deemed by the investigator to require a treatment with 30 - 200 U NT 201 for a treatment of up to three joints of the selected upper limb (wrist treatment mandatory).
  • Stable concomitant anti-tremor medication and no clinically relevant findings in routine laboratory examinations.

Main Exclusion Criteria:

  • Any neurological signs abnormal for the subject's age, other than the tremor itself and Froment's maneuver.
  • Exposure to the following tremorogenic drugs: Lithium, Valproic acid, Amiodarone, typical and atypical neuroleptics. Exposure to other than the listed tremorogenic or potentially tremorogenic drugs is allowed only if, in the opinion of the investigator, this will not interfere with the study drug evaluation. In these cases, a stable medication should be reached 4 weeks before screening and intended for the time during the study drug evaluation.
  • Trauma to the central nervous system or the nerves of the target limb within the three months preceding the onset of tremor.
  • Evidence of psychogenic origins of tremor.
  • Life habits (e.g. smoking, alcohol or substance abuse) prejudicial to study participation.
  • Prior surgery to treat tremor
  • Recent (16 weeks) treatment with any Botulinum toxin product for any reason.
  • Relevant recent or planned surgery or other specified relevant treatments and/or concomitant disorders.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02207946). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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