16 December 2025
Disclaimer: This is a simplified summary of a public company filing. See full disclaimer here.
Lomond Therapeutics Holdings, Inc.
CIK: 1900520•2 Annual Reports•Latest: 2025-04-15
10-K / April 15, 2025
Revenue:N/A
Income:-$17,100,000
10-K / April 1, 2024
Revenue:N/A
Income:-$47,936
10-K / April 15, 2025
Company Summary
Overview
- Name: Lomond Therapeutics Holdings, Inc. (formerly Venetian-1 Acquisition Corp.)
- Type: Biopharmaceutical company
- Focus: Discovery and development of therapeutics targeting hematological malignancies, primarily blood cancers such as Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS).
Business Activities
- Product Development: Currently advancing multiple drug candidates, including:
- Lomonitinib: A next-generation inhibitor targeting FLT3 and IRAK4 mutations relevant in AML and MDS.
- Licensed Products:
- Lonitoclax: A BCL-2 inhibitor licensed from Eil Therapeutics.
- Early-stage Menin inhibitors: Licensed from Bala Therapeutics.
- Research Approach: Uses structure-guided drug design combined with AI/ML platforms (specifically, large language models) to identify targeted therapies for cancers with resistance mutations.
- Pipeline Focus: Targets molecular driver oncogenes in hematologic cancers, especially FLT3 mutations, IRAK4, BCL-2, and Menin.
- Clinical Trials:
- Lomonitinib: In Phase 1b trial with initial data expected in Q2 2025.
- Lonitoclax: Preclinical and early clinical development underway, including a healthy volunteer study with initial data announced in Q4 2024.
- Menin inhibitors: Pending preclinical selection.
Intellectual Property
- Holds patent applications and licenses for its drug candidates.
- Licenses include rights to Lonitoclax (BCL-2 inhibitor) and menin inhibitors from Eil Therapeutics and Bala Therapeutics, respectively.
- Owns patents related to its lead candidate, Lomonitinib, with expiration dates around 2042-2044.
Market & Target Indications
- Focuses on hematological malignancies driven by mutations in FLT3, IRAK4, BCL-2, and Menin.
- Primary target is relapsed/refractory AML, especially FLT3-gatekeeper mutation cases which are resistant to existing FLT3 therapies.
- Estimated U.S. market for FLT3 AML patients: approximately 45,700 patients (7,700 previously treated and 38,000 untreated).
Operational & Financial Status
- Employees: No full-time employees; operations managed via an administrative services agreement.
- Revenue: None reported; company is early-stage with no products on the market.
- Income: Operating since 2020, has incurred significant net losses;
- 2024 net loss: $17.1 million
- 2023 net loss: $9.9 million
- Accumulated deficit (as of Dec 31, 2024): $38.8 million
- Cash & Equivalents (as of Dec 31, 2024): $28.4 million
- Revenue Model: Primarily through licensing rights, R&D grants, and collaborations, not from product sales.
Key Partnerships & Licensing
- Eil Therapeutics & Bala Therapeutics: Licenses for drug candidates, with related party arrangements.
- Viriom, Inc.: Licenses for additional molecules in Russia, involving related-party relationships.
Summary of Operations
- Focus on targeted oncology therapeutics specifically addressing drug resistance in hematologic cancers.
- Advanced clinical candidates with planned FDA and international regulatory filings.
- Relies on third-party manufacturing and collaborations for development and testing.
- No current sales, no products yet approved, and no revenue generated to date.
