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Search / Trial NCT00800332

Dose Finding Study With CYT003-QbG10 in Patients With House Dust Mite Allergy

Launched by CYTOS BIOTECHNOLOGY AG · Dec 1, 2008

Trial Information

Current as of June 05, 2025

Completed

Keywords

Rhinoconjunctivitis Due To House Dust Mite Allergy

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Perennial allergic rhinoconjunctivitis due to clinically relevant allergy towards house dust mite allergens
  • Further criteria as defined in the study protocol
  • Exclusion Criteria:
  • Clinically manifested seasonal allergy/-ies which is/are expected to interfere with the patient's study treatment schedule and/or assessments
  • Clinically relevant perennial allergy/-ies other than house dust mites allergy
  • Contraindication to any study test or procedure
  • Further criteria as defined in the study protocol

About Cytos Biotechnology Ag

Cytos Biotechnology AG is a biopharmaceutical company focused on the development of innovative therapeutic solutions for unmet medical needs. With a strong emphasis on harnessing the power of the immune system, Cytos is dedicated to advancing its proprietary technologies in the fields of vaccine development, immunotherapy, and targeted biologics. The company’s robust pipeline reflects its commitment to scientific excellence and patient-centric approaches, positioning it as a key player in the biotechnology landscape. Through strategic collaborations and a focus on clinical research, Cytos aims to bring transformative treatments to market, enhancing the quality of life for patients worldwide.

Locations

Paide, Tartu, Tallin, Rakvere, , Estonia

Fulda, Dresden, Ulm, Rodgau, Kassel, Eisenach, , Germany

Wiesbaden, Frankfurt/M, Leipzig, Jena, Hamburg, Dulmen, , Germany

N. Faliro, Hiraklion, Athens, , Greece

Riga, Rezekne, , Latvia

Vilnius, Kaunas, Klaipeda, , Lithuania

Galati, Cluj Napoca, Bahia Mare, Brasov, Piesti, , Romania

Targu Mures, Bukarest, Craiova, Iasi, , Romania

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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