Liuying Township, Taiwan Clinical Trials

A listing of Liuying Township, Taiwan clinical trials actively recruiting patients volunteers.

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Found 3381 clinical trials
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SPROUT - Pediatric Psoriasis - CC-10004 PPSO 003 - US  

This is a Phase 3, multicenter, randomized, placebo-controlled, double-blind study of the efficacy and safety of apremilast (CC-10004) in pediatric subjects with moderate to severe plaque psoriasis.

  • 12 views
  • 08 Jul, 2021
  • 20 locations
featured
  • 201 views
  • 23 Nov, 2020
  • 1 location
featured
Hereditary Angioedema (HAE)

An open-label study to evaluate the long-term safety of daily oral BCX7353 in subjects with Type I and Type II hereditary angioedema.

angioedema
  • 24 views
  • 14 May, 2020
  • 1 location
featured
A Randomized, Double-Blind, Double-Dummy, Active-Controlled Study Comparing the Efficacy, Safety and Tolerability of ABBV-951 to Oral Carbidopa/Levodopa in Advanced Parkinson's Disease Patients

The purpose of this study is to find out how well ABBV-951 works to control Parkinson's disease symptoms compared to oral Carbidopa (CD)/Levodopa (LD). The study is also seeking to test whether ABBV-951 is well tolerated in subjects with Parkinson's disease.

carbidopa
levodopa
  • 102 views
  • 23 Nov, 2020
  • 1 location
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CAHtalyst Study: A Research Study for Adults with Classic Congenital Adrenal Hyperplasia (CAH)

The CAHtalyst Study is a clinical research study evaluating an investigational medication for adults 18 years of age and older who have been diagnosed with classic congenital adrenal hyperplasia (CAH). The investigational medication is an oral capsule that will be taken twice daily with breakfast and evening meals. All participants who …

congenital adrenal hyperplasia
classic congenital adrenal hyperplasia
  • 30 views
  • 23 Nov, 2020
  • 1 location
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ECOSPOR IV: An Open-Label Extension of Study SERES-012 and Open-Label Program for Evaluating SER-109 in Adult Subjects with Recurrent Clostridioides difficile Infection (RCDI)

ECOSPOR IV is a Phase 3, multicenter, Open Label study to evaluate the safety and tolerability of SER-109 in adult subjects with recurrent CDI.

clostridium difficile
  • 41 views
  • 21 Dec, 2020
  • 77 locations
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A Phase 3, multicenter, randomized, double-blind, placebo-controlled, parallel-design study to assess the efficacy, safety, and tolerability of AVP-786 (deudextromethorphan hydrobromide [d6-DM]/quinidine sulfate [Q]) for the treatment of agitation in patients with dementia of the Alzheimer’s type.

Evaluate the efficacy, safety, and tolerability of AVP-786 compared to placebo, for the treatment of agitation in patients with dementia of the Alzheimer's type.  

agitation
dementia
memantine
donepezil
galantamine
  • 14 views
  • 08 Dec, 2020
  • 1 location
featured
Now Enrolling - Chronic Cough Research Study

A clinical research study for an investigational medication for Chronic Cough.  

  • 72 views
  • 20 Jul, 2021
  • 6 locations
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A Randomized, Multicenter, Double-Blind, Flexibly-dosed, Efficacy and Safety Study of Escitalopram in the Treatment of Children and Adolescents With Generalized Anxiety Disorder

The primary objective of this study is to assess the safety and efficacy of escitalopram relative to placebo in the acute treatment of children (aged 7 through 11 years) and adolescents (aged 12 through 17 years) who meet criteria for generalized anxiety disorder (GAD) as defined in the Diagnostic and …

  • 65 views
  • 23 Nov, 2020
  • 1 location
featured
Assessment of Efficacy and Safety of SPN-810 for the Treatment of Impulsive Aggression (IA) in Adolescent Subjects with Attention Deficit/Hyperactivity Disorder (ADHD) in Conjunction with Standard ADHD Treatment

Efficacy and safety of SPN-810 treatment in reducing the frequency of impulsive aggression (IA) behaviors in adolescents with ADHD when taken in conjunction with standard ADHD treatment.  

  • 32 views
  • 23 Nov, 2020
  • 1 location