SPY001 — Clinical data readout
in 2026
Part A: Open-label assessment of the safety and preliminary efficacy of a single dose level of each investigational monotherapy, with induction data expected in 2026.Source filing
catalyst calendar
SPYRE THERAPEUTICS INC · Data as of 2026-10-25
in 2026
Part A: Open-label assessment of the safety and preliminary efficacy of a single dose level of each investigational monotherapy, with induction data expected in 2026.Source filing
Q4 2026
Topline data for SPY072 in psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA) on track for Q4 2026 and for SPY072 in combination with IL17-A/F in hidradenitis suppurativa (HS) in late 2027 or early 2028Source filing
4Q 2026
All indications are expected to readout in 4Q 2026.Source filing
2027
Part B: Randomized and placebo-controlled assessment of the safety and efficacy of monotherapies and combinations, designed to provide dose-ranging data on monotherapies, proof-of-concept, and contribution of components for combinations, with induction data expected in 2027.Source filing
2027
SKYLINE Part B evaluating pairwise combinations of these components is enrolling with topline induction data expected in 2027Source filing
2027
We have begun enrolling these combinations globally and look forward to unveiling proof-of-concept data next year.Source filing
Sep 2027–Apr 2028
SKYLIGHT HS SPY072 + IL-17A/F Late 2027 or early 2028Source filing
Sep 2027–Apr 2028
Topline data for SPY072 in psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA) on track for Q4 2026 and for SPY072 in combination with IL17-A/F in hidradenitis suppurativa (HS) in late 2027 or early 2028Source filing
Sep 2026
Enrollment for Part A has completed, with SPY001 and SPY002 Part A topline induction data announced in Q2 2026, and topline data expected for SPY003 in September 2026.Source filing