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Clinical trials in Rivas-Vaciamadrid

2 clinical trials in Rivas-Vaciamadrid, Spain. Every trial is listed in the EU Clinical Trials Register and updated daily.

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Rivas-Vaciamadrid at a glance
2
clinical trials
  • Recruiting now0
  • Not yet recruiting0
  • Paediatric trials0
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2 trials in Rivas-Vaciamadrid

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Investigational
Countries:SpainSpain
  • Participants:18–64 years · 65+ years
  • Substances:Fezolinetant
  • Sponsor:Astellas Pharma Global Development Inc.
Registered drug
Countries:SpainSpain
  • Participants:0–17 years · 18–64 years · 65+ years
  • Substances:Albaconazole
  • Sponsor:Palau Pharma S.L.

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Clinical research in Rivas-Vaciamadrid

What the registry says about research in the country

01 Women's Health Research

Clinical investigations focusing on vulvovaginal conditions, specifically studying new therapeutic approaches for fungal infections affecting women's health. The research aims to evaluate innovative treatment options compared to existing standards of care.

  • Antifungal Therapy Development
  • Acute Candidiasis Treatment
  • Gynecological Health Solutions

These trials are exploring single-dose treatment options, potentially offering more convenient therapeutic solutions for patients dealing with acute fungal infections.

02 Infectious Disease Studies

Research centered on developing treatments for fungal infections, with a particular focus on comparing the effectiveness of different antifungal medications through controlled, double-blind studies.

  • Comparative Drug Analysis
  • Treatment Efficacy Assessment
  • Safety Profile Evaluation

The studies incorporate placebo-controlled methodologies to ensure robust scientific validation of new treatment approaches.

03 Clinical Pharmacology

Investigations into the pharmacokinetics of novel antifungal compounds, examining how different dosing strategies affect treatment outcomes and patient response.

  • Dose Optimization Research
  • Drug Safety Assessment
  • Clinical Response Analysis

These trials aim to establish optimal dosing protocols while maintaining high safety standards for new therapeutic agents.

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