Halia Therapeutics Presents Two AAIC 2026 Posters on HT-4253 for Alzheimer's Prevention in APOE4 Carriers

Preclinical data show HT-4253 reduces neuroinflammation and tau pathology; a second details a Phase 2a biomarker trial in pre-symptomatic APOE4 carriers via UAE genomics

LONDON, July 13, 2026 /PRNewswire/ -- Halia Therapeutics today announced two posters at the Alzheimer's Association International Conference (AAIC) 2026, July 12–15, linking preclinical data on its LRRK2 inhibitor HT-4253 to a biomarker trial to prevent or delay Alzheimer's disease (AD).

Halia's approach is grounded in genetic resilience: some APOE4 carriers, protected by a RAB10 variant, never develop Alzheimer's. HT-4253 reproduces that protection by inhibiting LRRK2, an upstream regulator of the RAB10 pathway.

"Our preclinical data show HT-4253 engages LRRK2, lowering neuroinflammation and tau phosphorylation and restoring microglial function," said David Bearss, Ph.D., CEO of Halia Therapeutics.

AAIC Presentations:

HT-4253, A Brain-Penetrant LRRK2 Inhibitor, Targets Neuroinflammation and Tau Pathology for AD Prevention in APOE4 Carriers

Wednesday, July 15, 2026, 7:30 a.m.–4:15 p.m.  •  Session: [In-Person Posters Wed] Drug Development: Human  •  Location: Exhibit Hall  •  Poster: Wednesday-0025 (Abstract #3245)

In human cell-based models, HT-4253 inhibited LRRK2 autophosphorylation and Rab10 phosphorylation, confirming target engagement. In iPSC-derived microglia (2D and 3D organoids), it reduced pro-inflammatory cytokine secretion; in iPSC-derived neurons, it decreased tau phosphorylation; and it restored phagocytic function in interferon-γ–exhausted BV2 microglia.

Design of a Phase 2a Trial of LRRK2 Inhibitor HT-4253 in Pre-symptomatic APOE4 Carriers Identified via Population-scale Genomics in the UAE

Monday, July 13, 2026, 7:30 a.m.–4:15 p.m.  •  Session: [In-Person Posters Mon] Drug Development: Human  •  Location: Exhibit Hall  •  Poster: Monday-0081 (Abstract #5843)

After a Phase 1 trial with a favorable safety profile, Halia designed an early-intervention study using population-scale UAE genomics to identify cognitively normal APOE4 carriers. Candidates are screened with C2N Diagnostics' PrecivityAD2™ blood test for elevated AD biomarkers signaling emerging amyloid pathology. Eligible participants enroll in a 48-week study of once-daily HT-4253, tracking blood-based biomarkers to assess whether it can alter disease onset and progression.

ABOUT HT-4253 AND THE LRRK2–RAB10 PATHWAY

HT-4253 is a brain-penetrant, small molecule inhibitor of leucine-rich repeat kinase 2 (LRRK2), a stress-recruited endolysosomal kinase that regulates membrane trafficking by phosphorylating Rab GTPases, including Rab10. Halia's hypothesis: persistent LRRK2 signaling, particularly in microglia, links major Alzheimer's pathologies: impaired lysosomal clearance, tau pathology, and chronic neuroinflammation.

ABOUT HALIA THERAPEUTICS

Halia Therapeutics, headquartered in Lehi, Utah and founded in 2017, is the genetic resilience company. Its secondary program, HT-4253, is in clinical development to prevent or delay Alzheimer's disease in APOE4 carriers. Halia's pipeline targets the RAB10 pathway through LRRK2 (upstream) and NEK7 (downstream) to regulate NLRP3 inflammasome activation, a driver of inflammation implicated in Alzheimer's, cancer, cardiovascular disease, and other chronic conditions.

Investor Contact
Leigh Salvo
New Street Investor Relations
leigh@newstreetir.com

Media Contact
Taylor Avei, Head of Business Development
Halia Therapeutics
tavei@haliatx.com • haliatx.com

شارك هذا المنشور

Preclinical data show HT-4253 reduces neuroinflammation and tau pathology; a second details a Phase 2a biomarker trial in pre-symptomatic APOE4 carriers via UAE genomics

LONDON, July 13, 2026 /PRNewswire/ -- Halia Therapeutics today announced two posters at the Alzheimer's Association International Conference (AAIC) 2026, July 12–15, linking preclinical data on its LRRK2 inhibitor HT-4253 to a biomarker trial to prevent or delay Alzheimer's disease (AD).

Halia's approach is grounded in genetic resilience: some APOE4 carriers, protected by a RAB10 variant, never develop Alzheimer's. HT-4253 reproduces that protection by inhibiting LRRK2, an upstream regulator of the RAB10 pathway.

"Our preclinical data show HT-4253 engages LRRK2, lowering neuroinflammation and tau phosphorylation and restoring microglial function," said David Bearss, Ph.D., CEO of Halia Therapeutics.

AAIC Presentations:

HT-4253, A Brain-Penetrant LRRK2 Inhibitor, Targets Neuroinflammation and Tau Pathology for AD Prevention in APOE4 Carriers

Wednesday, July 15, 2026, 7:30 a.m.–4:15 p.m.  •  Session: [In-Person Posters Wed] Drug Development: Human  •  Location: Exhibit Hall  •  Poster: Wednesday-0025 (Abstract #3245)

In human cell-based models, HT-4253 inhibited LRRK2 autophosphorylation and Rab10 phosphorylation, confirming target engagement. In iPSC-derived microglia (2D and 3D organoids), it reduced pro-inflammatory cytokine secretion; in iPSC-derived neurons, it decreased tau phosphorylation; and it restored phagocytic function in interferon-γ–exhausted BV2 microglia.

Design of a Phase 2a Trial of LRRK2 Inhibitor HT-4253 in Pre-symptomatic APOE4 Carriers Identified via Population-scale Genomics in the UAE

Monday, July 13, 2026, 7:30 a.m.–4:15 p.m.  •  Session: [In-Person Posters Mon] Drug Development: Human  •  Location: Exhibit Hall  •  Poster: Monday-0081 (Abstract #5843)

After a Phase 1 trial with a favorable safety profile, Halia designed an early-intervention study using population-scale UAE genomics to identify cognitively normal APOE4 carriers. Candidates are screened with C2N Diagnostics' PrecivityAD2™ blood test for elevated AD biomarkers signaling emerging amyloid pathology. Eligible participants enroll in a 48-week study of once-daily HT-4253, tracking blood-based biomarkers to assess whether it can alter disease onset and progression.

ABOUT HT-4253 AND THE LRRK2–RAB10 PATHWAY

HT-4253 is a brain-penetrant, small molecule inhibitor of leucine-rich repeat kinase 2 (LRRK2), a stress-recruited endolysosomal kinase that regulates membrane trafficking by phosphorylating Rab GTPases, including Rab10. Halia's hypothesis: persistent LRRK2 signaling, particularly in microglia, links major Alzheimer's pathologies: impaired lysosomal clearance, tau pathology, and chronic neuroinflammation.

ABOUT HALIA THERAPEUTICS

Halia Therapeutics, headquartered in Lehi, Utah and founded in 2017, is the genetic resilience company. Its secondary program, HT-4253, is in clinical development to prevent or delay Alzheimer's disease in APOE4 carriers. Halia's pipeline targets the RAB10 pathway through LRRK2 (upstream) and NEK7 (downstream) to regulate NLRP3 inflammasome activation, a driver of inflammation implicated in Alzheimer's, cancer, cardiovascular disease, and other chronic conditions.

Investor Contact
Leigh Salvo
New Street Investor Relations
leigh@newstreetir.com

Media Contact
Taylor Avei, Head of Business Development
Halia Therapeutics
tavei@haliatx.com • haliatx.com

halia-therapeutics-announces-positive-phase-2a-data-for-ofirnoflast-in-lower-risk-mds-at-ash-2025
halia-therapeutics-announces-presentation-at-the-bio-investment-growth-summit
halia-therapeutics-appoints-gary-sabin-as-executive-chairman-and-adds-three-independent-directors-to-board
halia-therapeutics-presents-two-aaic-2026-posters-on-ht-4253-for-alzheimers-prevention-in-apoe4-carriers
halia-therapeutics-receives-fda-fast-track-designation-for-ofirnoflast-ht-6184-in-lower-risk-myelodysplastic-syndromes
halia-therapeutics-to-present-final-phase-2-ofirnoflast-data-in-lower-risk-mds-at-eha2026-and-announces-appointment-of-han-myint-md-facp-as-chief-medical-officer
blog-title-heading-will-go-here-2
halia-therapeutics-ceo-dr-david-bearss-to-deliver-keynote-address-at-med-investment-forum-2025-in-abu-dhabi
halia-therapeutics-completes-enrollment-in-phase-2a-clinical-trial-of-ht-6184-for-myelodysplastic-syndrome-mds
halia-therapeutics-completes-first-in-human-phase-1-study-of-ht-4253-a-novel-lrrk2-inhibitor-targeting-neuroinflammation
halia-therapeutics-to-participate-in-the-morgan-stanley-23rd-annual-global-healthcare-conference
halia-therapeutics-strengthens-global-genomics-leadership-with-appointment-of-paul-jones-as-chief-strategy-officer-gm-international-markets
ofirnoflast-ht-6184-receives-orphan-drug-designation-from-u-s-fda-for-myelodysplastic-syndromes
halia-therapeutics-to-present-groundbreaking-data-on-novel-allosteric-nek7-inhibitor-ofirnoflast-at-the-2025-american-society-of-hematology-annual-meeting

حول هاليا ثيرابيوتك

Halia Therapeutics هي شركة أدوية بيولوجية في المرحلة السريرية تركز على علاج الأسباب الجذرية للالتهاب. من خلال الاستفادة من الرؤى الجينية والاكتشافات المدعومة بالذكاء الاصطناعي، تقوم Halia ببناء خط أنابيب قوي من العلاجات الجديدة القائمة على المرونة الجينية التي تستهدف المسارات الالتهابية في الأمراض التي تتراوح من الاضطرابات الأيضية إلى التنكّس العصبي والأورام الدموية الخبيثة.

تتمثل مهمة Halia في إنشاء علاجات تعتمد على البيانات لا تطيل العمر فحسب، بل تعمل أيضًا على تحسين جودتها. يقع المقر الرئيسي للشركة في ليهي بولاية يوتا، وتعمل بنشاط على تعزيز الشراكات العالمية في الأبحاث السريرية واكتشاف الأدوية والطب الشخصي.

لمعرفة المزيد، تفضل بزيارة www.haliatx.com أو تابعنا على لينكد إن وتويتر @HaliaTx.

جهة الاتصال الإعلامية

تايلور أفي، مدير تطوير الأعمال
علاجات هاليا

info@haliatx.com

الاتصال بالمستثمر

علاقات المستثمرين في لي سالفون-ستريت

leigh@newstreetir.com