Matches in Wikidata for { <http://www.wikidata.org/entity/Q63808822> ?p ?o ?g. }
Showing items 1 to 36 of
36
with 100 items per page.
- Q63808822 description "clinical trial" @default.
- Q63808822 description "ensayu clínicu" @default.
- Q63808822 description "klinisch onderzoek" @default.
- Q63808822 description "клінічне випробування" @default.
- Q63808822 name "Single Ascending Dose Study in Participants With LCA10" @default.
- Q63808822 type Item @default.
- Q63808822 label "Single Ascending Dose Study in Participants With LCA10" @default.
- Q63808822 prefLabel "Single Ascending Dose Study in Participants With LCA10" @default.
- Q63808822 P1050 Q63808822-72A1F19E-5AA8-46BF-A1B9-A32AC8B1A689 @default.
- Q63808822 P1050 Q63808822-E99C8752-E41D-4CE7-97AF-3222F27115F7 @default.
- Q63808822 P1132 Q63808822-E38FD256-08A3-4D18-A006-574EB4A289F9 @default.
- Q63808822 P1476 Q63808822-74D42495-BEA2-4284-B6C7-2A6C4952AD75 @default.
- Q63808822 P2899 Q63808822-C33CC225-7C22-41AA-B115-4680DF86F8C5 @default.
- Q63808822 P3098 Q63808822-6D1EE92F-9F86-462A-890F-2CFAE4ADC95D @default.
- Q63808822 P31 Q63808822-DF75044D-27B4-42EB-87AB-891EC849813A @default.
- Q63808822 P580 Q63808822-7345ECDF-DD68-43CF-A6CD-D6E34E84C0E2 @default.
- Q63808822 P582 Q63808822-19CB0418-1855-457C-9D69-C1B8BFBD9EB8 @default.
- Q63808822 P6099 Q63808822-0D74C6CB-313E-4152-A4AC-A48AB6F86079 @default.
- Q63808822 P6099 Q63808822-42F43F8D-F4B0-48DE-B2F0-6C302B6919EB @default.
- Q63808822 P6153 Q63808822-139DFA80-3D6A-4C14-A7CA-D4C434AF5A67 @default.
- Q63808822 P6153 Q63808822-A621F079-60D6-471D-8865-D6E5E5AF244B @default.
- Q63808822 P8363 Q63808822-2263C235-25B5-45C2-8285-FFABAC732DC6 @default.
- Q63808822 P1050 Q10874 @default.
- Q63808822 P1050 Q1811132 @default.
- Q63808822 P1132 "+18" @default.
- Q63808822 P1476 "Open-Label, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Efficacy of AGN-151587 (EDIT-101) in Adult and Pediatric Participants With Leber Congenital Amaurosis Type 10 (LCA10), With Centrosomal Protein 290 (CEP290)-Related Retinal Degeneration Caused by a Compound Heterozygous or Homozygous Mutation Involving c.2991+1655A>G in Intron 26 (IVS26) of the CEP290 Gene ("LCA10-IVS26")" @default.
- Q63808822 P2899 "+3" @default.
- Q63808822 P3098 "NCT03872479" @default.
- Q63808822 P31 Q30612 @default.
- Q63808822 P580 "2019-06-03T00:00:00Z" @default.
- Q63808822 P582 "2024-03-22T00:00:00Z" @default.
- Q63808822 P6099 Q42824440 @default.
- Q63808822 P6099 Q5452194 @default.
- Q63808822 P6153 Q4866339 @default.
- Q63808822 P6153 Q6784269 @default.
- Q63808822 P8363 Q78089383 @default.