Drugs / SCH 39641

Trials 7 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT03038971 Mar → Apr 2017 allergic rhinitis, conjunctivitis Woodmont Pharmaceuticals, Inc. Terminated No outcome recorded
Phase 21 trial
Phase 2 NCT00978029 Nov 2009 → Feb 2010 conjunctivitis, ragweed sensitivity, rhinitis ALK-Abelló A/S Completed No outcome recorded
Phase 2/31 trial
Phase 2/3 NCT00783198 Sep 2009 → May 2011 allergic rhinitis, conjunctivitis ALK-Abelló A/S Completed No outcome recorded
Phase 33 trials
Phase 3 NCT02676765 Jun 2016 → Jan 2018 Virginia Commonwealth University Terminated No outcome recorded
Phase 3 NCT02478398 Jul 2015 → Nov 2018 seasonal allergic rhinitis Merck Sharp & Dohme LLC Completed No outcome recorded
Phase 3 NCT01469182 Nov 2011 → Apr 2012 ragweed sensitivity ALK-Abelló A/S Completed No outcome recorded
Phase 41 trial
Phase 4 NCT02256553 Oct 2014 → Feb 2015 seasonal allergic rhinitis ALK-Abelló A/S Completed No outcome recorded

Press releases naming this drug 2 releases

DateIssuerRelease
2014-05-15 ALK-Abelló A/S ALK's partner for North America, Merck, announces launch of RAGWITEK™ in Canada alk.net
2014-04-17 ALK-Abelló A/S ALK announces FDA approval for Merck's ragweed sublingual allergy immunotherapy tablet RAGWITEK® alk.net

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as SCH 39641 ClinicalTrials.gov intervention name — accepted as the source's own label NCT00783198
2

NCT01469182

NCT00978029

Known as MK-3641 ClinicalTrials.gov intervention name — accepted as the source's own label NCT02256553
Known as Ragwitek RagwitekNCT02676765
Known as Short and Tall Ragweed Mix “Concentration 1: Short and Tall Ragweed MixNCT03038971
Known as Short ragweed pollen allergen extract ClinicalTrials.gov intervention name — accepted as the source's own label NCT02478398
Modality Protein / enzyme biologic “Biological: Short ragweed pollen allergen extract” NCT02478398
Route Other “One sublingual tablet containing 12 units of Amb a 1-U, once daily (QD) for up to 35 weeks.” NCT02478398