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Università degli studi Gabriele D’Annunzio Chieti-Pescara Centro di Studi e tecnologie avanzate

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Italy Via Luigi Polacchi 11, 66100 Chieti, Italy

  • 25 trials recruiting
  • Dermatitis atopic · Obesity · Type 2 diabetes mellitus
  • Adults and children

About Specializations

Università degli studi Gabriele D’Annunzio Chieti-Pescara Centro di Studi e tecnologie avanzate in Chieti, Italy specialises in clinical trials of conditions such as Dermatitis atopic, Obesity, Type 2 diabetes mellitus, Partial seizures, and other specialisations. This site conducts important research.

Main research areas of the site

Neurogenic Orthostatic Hypotension (nOH)

The medical center is at the forefront of research in Neurogenic Orthostatic Hypotension (nOH), a condition characterized by a significant drop in blood pressure upon standing, often associated with neurological disorders such as Multiple System Atrophy (MSA). The center's research focuses on innovative therapeutic approaches to manage and alleviate the symptoms of nOH, enhancing the quality of life for affected individuals.

  • Symptomatic Management
  • Therapeutic Efficacy
  • Durability of Treatment

Through rigorous clinical trials, the center evaluates the effectiveness and sustainability of novel treatments, contributing to the development of advanced therapeutic strategies for nOH. This research not only aims to improve patient outcomes but also to deepen the understanding of the underlying mechanisms of this complex condition.

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Site location
Via Luigi Polacchi 1166100 ChietiItaly
Recruiting now
25 trials
Conditions studied
49
Partner status
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Ongoing trials

Clinical trials currently enrolling participants at this site.

Condition
Type of trial
Recruitment status
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75 clinical trials

Obesity+2

Recruiting

Effect of zenagamtide on major adverse cardiovascular events in overweight or obese adults with established atherosclerotic cardiovascular disease

Investigational
Countries:ItalyItaly
  • Participants:18–64 years
  • Sponsor:Novo Nordisk A/S
Countries:ItalyItaly
  • Participants:18–64 years
  • Sponsor:Zenas Biopharma (USA) LLC

Orelabrutinib in Patients with Primary Progressive Multiple Sclerosis

Investigational
Countries:ItalyItaly
  • Participants:18–64 years
  • Sponsor:Zenas Biopharma (USA) LLC

Agitation+1

Recruiting

A study to evaluate the safety and effectiveness of dextromethorphan, deramciclane fumarate, and deramciclane in treating agitation in people with Alzheimer's disease

Investigational
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:Dextromethorphan Hydrobromide

Psoriasis

Recruiting

Long-term safety study of deucravacitinib compared to ustekinumab in adults with moderate to severe plaque psoriasis

Registered drugNo placebo
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:Deucravacitinib
  • Sponsor:Bristol-Myers Squibb Services Unlimited Company

Study on the Safety of BHV-7000 for Adults with Hard-to-Treat Focal Onset Epilepsy

InvestigationalNo placebo
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:BHV-7000
  • Sponsor:Biohaven Therapeutics Ltd.

Obesity

Recruiting

Long‑term Efficacy, Safety and Tolerability of maridebart cafraglutide in Adults with Obesity and Type 2 Diabetes

Investigational
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:Maridebart Cafraglutide
  • Sponsor:Amgen Inc.

Obesity+1

Recruiting

A Phase 3 Study of Once‑Monthly PF‑08653944 vs Placebo for Weight Loss in Adults with Overweight or Obesity

Investigational
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Sponsor:Pfizer Inc.

Depression

Recruiting

Safety and dose‑finding study of trazodone hydrochloride and psilocybin in patients with treatment‑resistant depression

Registered drugNo placebo
Countries:ItalyItaly
  • Participants:18–64 years
  • Substances:Dry Extract From Psilocybe Cubensis (15-25:1), Extraction Solvent: Methanol
  • Sponsor:Universita' Degli Studi G. D'Annunzio Di Chieti
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:Gadoteric Acid

Hidradenitis

Recruiting

A safety and efficacy study of SAR445399 in adults with moderate to severe hidradenitis suppurativa

Investigational
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:SAR445399
  • Sponsor:Sanofi-Aventis Recherche & Developpement

A study to evaluate the effectiveness and safety of remibrutinib in patients with secondary progressive multiple sclerosis

Investigational
Countries:ItalyItaly
  • Participants:18–64 years · 65+ years
  • Substances:Remibrutinib
  • Sponsor:Novartis Pharma AG
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