Other Clinical Trial - Safety & Tolerance Study of Grass Pollen-derived

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Conjunctivitis
Conjunctivitis, Allergic
Seasonal Allergic Rhinoconjunctivitis

See also
Status	Clinical Trial	Phase
Completed	`NCT01111279` - Clinical Safety and Tolerability Study of gpASIT+TM and gpASIT+TM/Immunoregulating Adjuvant to Treat Seasonal Grass Pollen Rhinoconjunctivitis	Phase 1
Completed	`NCT00833066` - Safety Study of Grass Pollen-derived Peptides to Treat Seasonal Allergic Rhinoconjunctivitis	Phase 1/Phase 2
Completed	`NCT02761252` - Efficacy of Co-administration of Bilastine and Montelukast in Patients With SARC and Asthma	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT01111279 - Clinical Safety and Tolerability Study of gpASIT+TM and gpASIT+TM/Immunoregulating Adjuvant to Treat Seasonal Grass Pollen Rhinoconjunctivitis

Phase 1

Completed

NCT00833066 - Safety Study of Grass Pollen-derived Peptides to Treat Seasonal Allergic Rhinoconjunctivitis

Phase 1/Phase 2

Completed

NCT02761252 - Efficacy of Co-administration of Bilastine and Montelukast in Patients With SARC and Asthma

Phase 4

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00813046
Study type	Interventional
Source	BioTech Tools S.A.
Contact
Status	Completed
Phase	Phase 1
Start date	December 2008
Completion date	January 2009

Safety and Tolerance Study of Grass Pollen-derived Peptides to Treat Allergic Rhinitis

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms