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Spots Global Cancer Trial Database for Efficacy and Safety Study of Benralizumab for Patients With Severe Nasal Polyposis

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Trial Identification

Brief Title: Efficacy and Safety Study of Benralizumab for Patients With Severe Nasal Polyposis

Official Title: A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Phase 3 Efficacy and Safety Study Of Benralizumab in Patients With Severe Nasal Polyposis

Study ID: NCT03401229

Conditions

Nasal Polyposis

Study Description

Brief Summary: The aim of this present study is to investigate the use of benralizumab as treatment for severe nasal polyposis. The effect of benralizumab on nasal polyps will be assessed over a 56 weeks of treatment period in patients with severe bilateral nasal polyposis who are still symptomatic despite standard of care therapy, i.e current use of intranasal corticosteroids (INCS) and prior surgery and/or use of systemic corticosteroids. The first 200 patients that complete the 56-week treatment will have a 6 month follow-up (FU) period without dosing.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Birmingham, Alabama, United States

Research Site, Fresno, California, United States

Research Site, Huntington Beach, California, United States

Research Site, La Mesa, California, United States

Research Site, Los Angeles, California, United States

Research Site, Los Angeles, California, United States

Research Site, Orange, California, United States

Research Site, Roseville, California, United States

Research Site, Walnut Creek, California, United States

Research Site, Centennial, Colorado, United States

Research Site, Glenwood Springs, Colorado, United States

Research Site, Washington, District of Columbia, United States

Research Site, Lake Mary, Florida, United States

Research Site, Atlanta, Georgia, United States

Research Site, Decatur, Georgia, United States

Research Site, Chicago, Illinois, United States

Research Site, Chicago, Illinois, United States

Research Site, Des Moines, Iowa, United States

Research Site, Kansas City, Kansas, United States

Research Site, Louisville, Kentucky, United States

Research Site, Baltimore, Maryland, United States

Research Site, Boston, Massachusetts, United States

Research Site, Boston, Massachusetts, United States

Research Site, Rochester, Minnesota, United States

Research Site, Lincoln, Nebraska, United States

Research Site, Bronx, New York, United States

Research Site, Hewlett, New York, United States

Research Site, New Windsor, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, Plainview, New York, United States

Research Site, White Plains, New York, United States

Research Site, Charlotte, North Carolina, United States

Research Site, Winston-Salem, North Carolina, United States

Research Site, Oklahoma City, Oklahoma, United States

Research Site, Philadelphia, Pennsylvania, United States

Research Site, Pittsburgh, Pennsylvania, United States

Research Site, Charleston, South Carolina, United States

Research Site, Conroe, Texas, United States

Research Site, Houston, Texas, United States

Research Site, North Logan, Utah, United States

Research Site, Norfolk, Virginia, United States

Research Site, Richmond, Virginia, United States

Research Site, Spokane, Washington, United States

Research Site, Graz, , Austria

Research Site, Linz, , Austria

Research Site, Salzburg, , Austria

Research Site, St. Pölten, , Austria

Research Site, Wien, , Austria

Research Site, Bruxelles, , Belgium

Research Site, Gent, , Belgium

Research Site, Leuven, , Belgium

Research Site, Vancouver, British Columbia, Canada

Research Site, Hamilton, Ontario, Canada

Research Site, London, Ontario, Canada

Research Site, Mississauga, Ontario, Canada

Research Site, Ottawa, Ontario, Canada

Research Site, Montreal, Quebec, Canada

Research Site, Montreal, Quebec, Canada

Research Site, Montreal, Quebec, Canada

Research Site, Trois-Rivières, Quebec, Canada

Research Site, Quebec, , Canada

Research Site, Quebec, , Canada

Research Site, Aalborg, , Denmark

Research Site, Aarhus N, , Denmark

Research Site, Hillerød, , Denmark

Research Site, Hvidovre, , Denmark

Research Site, København NV, , Denmark

Research Site, Køge, , Denmark

Research Site, Næstved, , Denmark

Research Site, Odense C, , Denmark

Research Site, Vejle, , Denmark

Research Site, Aschaffenburg, , Germany

Research Site, Berlin, , Germany

Research Site, Dreieich, , Germany

Research Site, Dresden, , Germany

Research Site, Düsseldorf, , Germany

Research Site, Göttingen, , Germany

Research Site, Heidelberg, , Germany

Research Site, Lübeck, , Germany

Research Site, Münster, , Germany

Research Site, Wiesbaden, , Germany

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Debrecen, , Hungary

Research Site, Eger, , Hungary

Research Site, Nyíregyháza, , Hungary

Research Site, Pécs, , Hungary

Research Site, Veszprém, , Hungary

Research Site, Nadarzyn, , Poland

Research Site, Strzelce Opolskie, , Poland

Research Site, Warszawa, , Poland

Research Site, Wrocław, , Poland

Research Site, Wrocław, , Poland

Research Site, Łódź, , Poland

Contact Details

Name: Claus Bachert, Prof. dr. h.c.

Affiliation: University Hospital Ghent, de Pintelaan 185, 9000 Ghent, Belgium

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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