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Inhibikase Therapeutics (IKT) investor relations material
Inhibikase Therapeutics Q3 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
IMPROVE-PAH, the pivotal global Phase 3 study of IKT-001 for PAH, had approvals in 28 countries and 79 of 180 planned sites activated; an interim Part A safety readout in 50 patients is planned for H1 2027.
FDA granted IKT-001 Orphan Drug Designation in July 2026, potentially providing clinical-trial tax credits, fee exemptions and seven years of market exclusivity upon approval.
Financial highlights
Q3 2026 net loss was $20.5M, or $0.10/share, vs. $11.9M, or $0.13/share, in Q3 2025; 9M net loss was $56.4M, or $0.31/share, vs. $35.5M, or $0.40/share.
Q3 R&D expense rose to $15.0M from $7.6M; 9M R&D was $39.2M vs. $23.4M, with 2025 including a $7.4M noncash IPR&D write-off and $1.8M CorHepta-related stock compensation.
Q3 SG&A was $7.2M vs. $5.6M; 9M SG&A was $22.3M vs. $16.8M. Higher stock-based compensation and personnel costs contributed to the increase; 2025 included $1.0M in severance for former senior executives.
Other income was $1.8M in Q3 and $4.7M for 9M, driven by interest on cash, cash equivalents and marketable securities.
Outlook and guidance
Existing cash, cash equivalents and marketable securities were expected to fund operations for at least 12 months after the report date; funding through Part B topline data assumes full, timely exercise of outstanding Series A and B warrants and projected development timelines.
Part A plans ~140 patients, with change in PVR at Week 24 as the primary endpoint; Part B plans ~346 patients, with change in 6MWD at Week 24 as the primary endpoint, and is to begin after Part A's last patient enrolls.
R&D expense is expected to rise for several years as IKT-001 advances and regulatory approval is pursued; substantial additional funding is anticipated. Estimated remaining CRO and CMO contract costs were $107.6M and $8.7M, primarily through 2030.
Nonclinical results for sotatercept combination studies are expected progressively from Q1 2027; Group 2 studies during 2027 and Group 3 studies in late 2027 or early 2028.
- IKT-001 pairs imatinib’s PAH efficacy potential with a redesigned Phase 3 program.IKT
Corporate presentation - IKT-001 targets PAH with strong efficacy, improved tolerability, and global Phase 3 enrollment underway.IKT
Corporate presentation - IKT-001 targets PAH with improved tolerability and efficacy; Phase 3 topline data expected 2029.IKT
Corporate presentation - Phase 3 PAH trial advances, Orphan Drug Designation secured, and $50M raised in July 2026.IKT
Q2 2026 - Q1 2026 net loss reached $16.4M as global Phase 3 PAH trial enrollment and spending increased.IKT
Q1 2026 - Director elections, auditor ratification, and equity plan amendments headline the annual meeting.IKT
Proxy filing - Virtual annual meeting to vote on directors, auditor, equity plan, and executive pay proposals.IKT
Proxy filing - Virtual meeting to vote on directors, auditor, equity plan, and executive compensation matters.IKT
Proxy filing - IKT-001 targets PAH with improved tolerability and efficacy, aiming for first-in-class oral approval.IKT
Corporate presentation
Next Inhibikase Therapeutics earnings date
Next Inhibikase Therapeutics earnings date
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