Inhibikase Therapeutics
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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.
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Q3 2026 earnings summary10 Nov, 2026

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.

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Jefferies Global Healthcare Conference16 Nov, 2026
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Frequently asked questions

Inhibikase Therapeutics Inc. is a biopharmaceutical company focused on developing treatments for neurodegenerative diseases and cancers. The company’s research primarily targets diseases related to protein misfolding, such as Parkinson's disease, by aiming to inhibit the malfunction of key cellular processes. Inhibikase Therapeutics develops therapeutics that aim to modify the progression of these diseases and improve patient outcomes. Its approach includes addressing both neurological and oncological conditions through small-molecule therapeutics. The company is headquartered in Atlanta, Georgia, and its shares are listed on the NASDAQ.