NEW YORK, Jan. 2, 2025 /PRNewswire/ -- PieX AI, a global leader in multimodal AI hardware for smart health, is set to proudly launch the world's first pendant featuring personalized, on-device AI at CES 2025. This innovative product aims to revolutionize mental health management by seamlessly integrating technology with emotional well-being.
A Focus on Mental Health
PieX's mission is to enhance users' mental health through advanced applications such as AI life coaching, guided breathing exercises, and comprehensive health monitoring. The PieX pendant is a holistic tool that applies physiological and psychological to support emotional well-being. By empowering users to recognize and embrace their feelings, PieX promotes users to build a positive mindset, ultimately enhancing their mental energy and well-being.
Proprietary Sensing and AI Technology
The PieX pendant is built upon our proprietary Sensing Technology and foundation models featuring both Personalized AI and On-device AI. The sensing technology provides 24/7 accurate emotion tracking results to build a personalized emotion database for each user, making the AI know users better. Moreover, the AI running on users' own phones ensures that users' emotional data and auto-journaled information are processed and stored locally, eliminating the need for cloud storage. This feature provides an ultimate solution to enhance user privacy and data security in the LLM era.
- Sensing Tech: The pendant's sensing capability not only accurately measures indicators of stress, such as the wearer's HRV (heart rate variability), but also precisely assesses the user's emotional state through their speech tone during conversation. By combining these two aspects, it provides users with a comprehensive emotional tracking insight. Moreover, the pendant's sensing ability also offers users the capacity to perceive their environment and events, correlating emotional states with daily occurrences, thus helping users better cope with various emotional changes.
- AI Tech: Leveraging the exceptional sensing capabilities of the pendant, our device will provide a personalized AI that understands the user best. It can automatically offer options for meditation and breathing exercises based on the user's emotional changes and preferences, enabling users to take a more proactive approach to their mental health. Additionally, all emotional sensing and data processing analysis occur solely on the user's personal device, with no need for cloud uploads. Even large language models run locally, ensuring that sensitive information never leaves the user's devices.
PieX AI at CES: Booth #63001-02,Level 1,Hall G, Venetian Expo.
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PieX AI: Launching the World's First Personalized, On-device AI Pendant at CES 2025
Australia's Therapeutic Goods Administration (TGA), responsible for approval of the safety, quality, and efficacy of therapeutic goods, has determined that Skyhawk's SKY-0515 orally-administered small molecule therapy for the treatment of Huntington's disease meets TGA eligibility criteria for registration via the provisional approval pathway.
Skyhawk delivered its application for provisional approval to the TGA today.
More than 115 patients are now on trial with SKY-0515.
BOSTON, March 3, 2026 /PRNewswire/ -- Skyhawk Therapeutics, Inc., a clinical-stage biotechnology company developing novel small molecule therapies designed to modulate critical RNA targets for a series of challenging neurological diseases, announces that Australia's Therapeutic Goods Administration (TGA), responsible for the approval of the safety, quality, and efficacy of therapeutic goods, has determined that the Company's SKY-0515 orally-administered small molecule therapy for the treatment of Huntington's disease meets TGA eligibility criteria for registration via the provisional approval pathway.
Skyhawk delivered its application submission to the TGA for provisional approval today.
"We are grateful that the TGA has determined SKY-0515 for the treatment of Huntington's disease meets its eligibility criteria for potential provisional approval," said Bill Haney, Skyhawk's CEO. "This represents an important first step toward what could be an accelerated path to approval in Australia and the world, offering the possibility of a disease modifying treatment for Huntington's patients who urgently need therapies for this devastating disease."
Treatment with SKY-0515 results in dose-dependent reductions of mHTT and PMS1, key drivers of Huntington's disease pathology. SKY-0515 has demonstrated excellent central nervous system exposure and been generally safe and well tolerated.
Patients receiving SKY-0515 in the Phase 1C trial of SKY-0515 demonstrate mean Composite Unified Huntington's Disease Rating Scale (cUHDRS) improvement from baseline. At nine months this improvement is +0.64 points in a pooled analysis, compared to expected worsening at nine months of cUHDRS in symptomatic patients of -0.73 points, based on propensity score weighting using Enroll-HD and TRACK-HD.
Huntington's disease is a rare, inherited and ultimately fatal neurodegenerative disorder that affects hundreds of thousands of people worldwide, including more than 40,000 symptomatic patients in the United States and over 2,000 Australians.1,2 There are currently no approved disease-modifying treatments which slow or halt disease progression.2
SKY-0515 is a small molecule RNA splicing modifier developed through Skyhawk's novel RNA-splicing platform, SKYSTAR®.
SKY-0515 is the first Skyhawk drug in clinical trials.
Skyhawk is developing additional novel drugs to treat neurological diseases for which there are no approved disease-modifying therapies.
About SKY-0515's Phase 1 Clinical Study
SKY-0515's Phase 1 clinical trial is a first-in-human trial designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of SKY-0515 in healthy volunteers and individuals with Huntington's disease (HD). The trial is separated into three parts. Parts A and B evaluated SKY-0515 in Healthy Volunteers. Part C is a double-blind placebo-controlled parallel design study of two dose levels of SKY-0515 and placebo in individuals with HD (HD-ISS Stage 1, 2, or mild Stage 3) for 84 days followed by a 12 month extension of active treatment where all participants receive either a low or high dose of SKY-0515 in a blinded fashion. The objectives of the study include evaluating mutant HTT protein and PMS1 mRNA. The first patients were dosed in SKY-0515's Part C in January 2025. Enrollment in Phase 1C of the SKY-0515 trial is now complete and the trial is ongoing.
About SKY-0515's Phase 2/3 FALCON-HD Clinical Study
FALCON-HD (NCT06873334) is a Phase 2/3 randomized, double-blind, placebo-controlled, dose ranging study to evaluate the pharmacodynamics, safety, and efficacy of SKY-0515 in 120 participants with Stage 2 and early Stage 3 HD across 12 sites in Australia and New Zealand, and 400 participants with Stage 2 and early Stage 3 HD in 40+ worldwide sites. Eligible patients will receive a once-daily oral dose of SKY-0515 at one of three dose levels or placebo, for a treatment period of at least 12 months. This trial aims to confirm the potential of SKY-0515 to modulate RNA splicing and reduce mHTT and PMS1 proteins, which are implicated in the pathology of Huntington's disease, and to assess the efficacy of the SKY-0515 in affecting the rate of Huntington's disease progression. Additional information about FALCON-HD, including participating sites and eligibility criteria, can be found at ClinicalTrials.gov and www.FALCON-HD.com.
About Skyhawk Therapeutics
Skyhawk Therapeutics is a clinical-stage biotechnology company which uses its proprietary platform, SKYSTAR®, to discover and develop small molecule RNA modulating therapies for the world's most intractable diseases. For more information visit www.skyhawktx.com.
Skyhawk Contact
Maura McCarthy
Head of Corporate Development
maura@skyhawktx.com
References
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Skyhawk Announces Australia's Therapeutic Goods Administration Has Determined SKY-0515 for Huntington's Disease Meets Eligibility Criteria for Registration via the Provisional Approval Pathway
