ZyppBe schreef op 17 januari 2021 13:29:
Update:
2021UC (Ulcerative colitis)*JAP filing 1H21
*EU opinion 1H21 (CHMP)
*EU approval decision 2H21 (EC)
*US filing in UC contingent on MANTA safety data
*US filing potentially 1H22 for launch 2023. (in best case filing in 2H21)
MANTA / MANTA-RAy*26-week readouts expected by mid-2021
*FDA requesting up to week-52 data in patients that show >50% decrease in semen parameters by week-26 and do not recover.
*If 52-week follow up sperm count data are required after all, it can further delay US filings and scrutinize both US and ex-US regulators regarding filgotinib’s safety profile. (definitive data 1H22)
FIBROSIS / IPF*GLPG1690 futility analysis ISABELA trails (ziritaxestat) 1H21
*GLPG1205 showed FVC benefit in PINTA (~60 patients)
Preparing Phase 2b dose range finder, to start in 2021
*GLPG4716 (OATD-01 OncoArendi)
Preparing Phase 2b study (~200 patients)
*Preclinical IPF assets:
GLPG4586 (Undisclosed target)
GLPG4605 (SIK2/3)
Other (7 novel targets)
TOLEDO*GLPG3970 expect toplines from the first three PoC in mid-2021 (with additional Ph1 starts and a potential IND opening )
*GLPG3970 three PoC studies: CALOSOMA in psoriasis, SEA TURTLE in ulcerative colitis, and LADYBUG in rheumatoid arthritis
*GLPG4399 (SIK3) expect a readout of Ph1 in 2021 followed by the initiation of Phase 2b studies
OA (Osteoarthritis)*Readout GLPG555 (JAK1) Phase 1b
PsA(Psoriasis) *Readout GLPG3667 (TYK2) Phase 1b
*Readout GLPG3970 PoC CALOSOMA (TOLEDO)
CD (Crohn’s Disease)*DIVERSITY recruited 2H21.
2022MANTA / MANTA-RAy*52-week follow up data in 1H22
UC (Ulcerative colitis)*JAP approval decision 1H22
*Possible US filing (contingent on MANTA safety data)
IPF*GLPG1690 full readout ISABELA trails (ziritaxestat) 1H22.
TOLEDO*GLPG3970 expect readouts from last 2 PoC: TAPINOMA in Systemic lupus erythematosus, and GLIDER Primary Sjögren's syndrome
*Additional Ph1 readouts
CD (Crohn’s Disease)*Data from the Phase III DIVERSITY trial are expected in 2022.
Aims to build on the phase 2 FITZROY study.
*Potential filing EU + JAP in 2H22
*Potential approval date 2023