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Trial · NCT03575676

Efficacy and Safety of SOM3355 in Huntington's Disease Chorea

NCT03575676, Phase 2, Completed, SOM Innovation Biotech SA

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Efficacy and Safety of SOM3355 in Huntington's Disease Chorea. Trials, record NCT03575676. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03575676

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Efficacy and Safety of SOM3355 in Huntington's Disease Chorea
NCT number
NCT03575676
Status
Completed
Phases
Phase 2
Enrollment
32 participants, actual
Lead sponsor
SOM Innovation Biotech SA
Conditions
Huntington's Chorea
Interventions
SOM3355 100mg BID, SOM3355 200mg BID, Placebo BID
First posted
2018-07-02
Last updated
2019-09-16
Other registries' IDs
eudract:2018-000203-16

Source ClinicalTrials.gov

Registered outcomes9

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryUHDRS (Unified Huntington's Disease Rating Scale) Total Maximal Chorea (TMC) score6 monthsUHDRS subscore used to measure the effectiveness of SOM3355 on HD chorea.
SecondaryClinical Global Impression of Change (CGIC) scale6 monthsPGIC reflects clinician's belief about the efficacy of treatment.
SecondaryPatient Global Impression of Change (PGIC) scale6 monthsPGIC reflects a patient's belief about the efficacy of treatment.
SecondaryUHDRS Total Functional Capacity (TFC)6 monthsA standardized rating scale used to assess capacity to work, handle finances, perform domestic chores and self-care tasks.
SecondaryUHDRS Functional Assessment6 monthsFunctional Assessment should be judged according to the investigator's opinion of capacity to perform the activity rather than the actual performance of this activity.
SecondaryUHDRS Gait score6 monthsUHDRS subscore used to assess patient's gait.
SecondaryUHDRS Total Motor Score (TMS)6 monthsCategoric clinical rating scale assessing multiple domains of motor disability in HD.
SecondaryColumbia Suicide Severity Rating Scale (C-SSRS)6 monthsInternational validated questionnaire used for suicide assessment.
SecondarySafety (number of participants with adverse events)6 months
The maximum grade for each type of AE will be recorded for each subject, and frequency tables will be presented and reviewed to determine patterns. The relationship of the AE to the study treatment will be taken into consideration. Hypotension and cardiovascular events will be specifically analyzed.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

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

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
36494329DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03575676

GET https://conductscience.org/api/trials/v1/NCT03575676/registered