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Lomond Therapeutics Holdings, Inc.

CIK: 19005202 Annual ReportsLatest: 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.