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HDAX Therapeutics

HDAX is developing small molecules that utilize a novel two-site binding mechanism to target HDAC6, a key protein involved in microtubule stability and inflammatory processes. This approach addresses the limitations of conventional drug design by enhancing efficacy and safety for treating neuropathies and cardiovascular diseases.

Traction 10/10
Boston, United States · HQ
Founded 2023153K+ followers
  • Biotechnology
Updated 23 months ago

Funding

Raised to date

$5.4MRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.

Funding rounds are not available yet.

Founders

2 founders

Nabanita Nawar

Co-Founder/CEO

Pimyupa Manaswiyoungkul

Co-Founder/COO

Product

Problem

Conventional drug design often struggles to effectively target disease-driving proteins, leading to limited efficacy and challenges in translating research into meaningful treatments for patients. This is particularly true for complex targets like HDAC6, where achieving both high potency and selectivity has been difficult.

Solution

HDAX is developing a new class of small molecule therapeutics that target HDAC6 using a proprietary two-site binding mechanism. This innovative approach enhances both the efficacy and safety profiles of their drug candidates. By selectively modulating HDAC6, HDAX aims to address the limitations of first-generation medicines and unlock the full therapeutic potential of HDAC6 inhibition for diseases with limited treatment options. Their technology broadens dosing regimens and improves pharmacokinetics, potentially leading to life-changing treatments for debilitating diseases.

Target Audience

The primary target audience includes patients suffering from neuropathies, cardiovascular diseases, and other conditions where HDAC6 modulation can provide therapeutic benefit, as well as pharmaceutical companies seeking innovative drug candidates with improved efficacy and safety profiles.

Features

  • Novel 2-site binding mechanism for enhanced HDAC6 selectivity and potency
  • Improved drug-like features, including enhanced efficacy, pharmacokinetics, and safety profile
  • Potential for multi-indication applications due to HDAC6's involvement in cytoskeleton dynamics, microtubule stability, and inflammatory processes
  • Small molecule therapeutics designed to overcome the limitations of traditional drug design approaches
This profile is AI-generated and may contain inaccuracies.