Hereditary ATTR (hATTR) Amyloidosis Pipeline Insights 2025: EMA, PDMA, FDA Approvals, Mechanism of Action, ROA, NDA

DelveInsight's, "Hereditary Transthyretin Amyloidosis Pipeline Insight" report provides comprehensive insights about 8+ companies and 8+ pipeline drugs in Hereditary Transthyretin Amyloidosis (hATTR) pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

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Key Takeaways from the Hereditary ATTR (hATTR) Amyloidosis Pipeline Report
• DelveInsight's Hereditary ATTR (hATTR) Amyloidosis pipeline report depicts a robust space with 8+ active players working to develop 8+ pipeline therapies for Hereditary ATTR (hATTR) Amyloidosis treatment.
• The leading Hereditary ATTR (hATTR) Amyloidosis Companies such as Alnylam Pharmaceuticals, Ionis Pharmaceuticals, Eidos Therapeutics, Intellia Therapeutics, Corino Therapeutics, Novo Nordisk and others.
• Promising Hereditary ATTR (hATTR) Amyloidosis Therapies such as Patisiran, Vutrisiran, ION-682884, Eplontersen and others.

Discover how the Hereditary ATTR (hATTR) Amyloidosis treatment paradigm is evolving. Access DelveInsight's in-depth Hereditary ATTR (hATTR) Amyloidosis Pipeline Analysis for a closer look at promising breakthroughs @ https://www.delveinsight.com/sample-request/hereditary-transthyretin-amyloidosis-hattr-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=ypr

Hereditary Transthyretin Amyloidosis (hATTR) Emerging Drugs

• Vutrisiran: Alnylam Pharmaceuticals
Vutrisiran is an investigational, subcutaneously administered RNAi therapeutic in development for the treatment of ATTR amyloidosis, which encompasses both hereditary (hATTR) and wild-type (wtATTR) amyloidosis. It is designed to target and silence specific messenger RNA, blocking the production of wild-type and variant transthyretin (TTR) protein before it is made. Quarterly administration of vutrisiran may help to reduce deposition and facilitate the clearance of TTR amyloid deposits in tissues and potentially restore function to these tissues. Vutrisiran utilizes Alnylam's Enhanced Stabilization Chemistry (ESC)-GalNAc-conjugate delivery platform, designed for increased potency and high metabolic stability that allows for infrequent subcutaneous injections. HELIOS-B is a randomized, double-blind, placebo-controlled Phase 3 study of ~600 adult patients with ATTR amyloidosis with cardiomyopathy (including both hATTR and wtATTR amyloidosis). The U.S. Food and Drug Administration (FDA) has accepted the Company's New Drug Application (NDA) for vutrisiran, an investigational RNAi therapeutic for the treatment of the polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adults. The FDA has set an action date of April 14, 2022 under the Prescription Drug User Fee Act (PDUFA), and the Agency has indicated that they are not currently planning an advisory committee meeting as part of the NDA review.

• AKCEA-TTR-LRx: Ionis Pharmaceuticals
AKCEA-TTR-LRx is an antisense drug developed using Ionis' proprietary LIgand Conjugated Antisense (LICA) technology platform and is designed to inhibit production of TTR. It was discovered by Ionis and is being co-developed by Ionis and Akcea. In a Phase 1 clinical trial, patients treated with AKCEA-TTR-LRx experienced reductions in TTR of up to 94 percent at the highest dose. CARDIO-TTRansform is a global, double-blind, randomized, placebo-controlled Phase III cardiovascular outcome study. It is designed to compare AKCEA-TTR-LRx to placebo in patients with both wild type and hereditary ATTR cardiomyopathy who are on the current available standard of care.

The Hereditary ATTR (hATTR) Amyloidosis pipeline report provides insights into
• The report provides detailed insights about companies that are developing therapies for the treatment of Hereditary ATTR (hATTR) Amyloidosis with aggregate therapies developed by each company for the same.
• It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Hereditary ATTR (hATTR) Amyloidosis Treatment.
• Hereditary ATTR (hATTR) Amyloidosis Companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
• Hereditary ATTR (hATTR) Amyloidosis Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type.
• Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Hereditary ATTR (hATTR) Amyloidosis market.

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Hereditary ATTR (hATTR) Amyloidosis Companies
Alnylam Pharmaceuticals, Ionis Pharmaceuticals, Eidos Therapeutics, Intellia Therapeutics, Corino Therapeutics, Novo Nordisk and others.

Hereditary Transthyretin Amyloidosis (hATTR) pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
• Oral
• Parenteral
• Intravenous
• Subcutaneous
• Topical
• Molecule Type

Hereditary ATTR (hATTR) Amyloidosis Products have been categorized under various Molecule types such as
• Monoclonal Antibody
• Peptides
• Polymer
• Small molecule
• Gene therapy
• Product Type

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Scope of the Hereditary ATTR (hATTR) Amyloidosis Pipeline Report
• Coverage- Global
• Hereditary ATTR (hATTR) Amyloidosis Companies- Alnylam Pharmaceuticals, Ionis Pharmaceuticals, Eidos Therapeutics, Intellia Therapeutics, Corino Therapeutics, Novo Nordisk and others.
• Hereditary ATTR (hATTR) Amyloidosis Therapies- Patisiran, Vutrisiran, ION-682884, Eplontersen and others.
• Hereditary ATTR (hATTR) Amyloidosis Therapeutic Assessment by Product Type: Mono, Combination, Mono/Combination
• Hereditary ATTR (hATTR) Amyloidosis Therapeutic Assessment by Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III

Which companies are leading the race in Hereditary ATTR (hATTR) Amyloidosis drug development? Find out in DelveInsight's exclusive Hereditary ATTR (hATTR) Amyloidosis Pipeline Report-access it now! @ https://www.delveinsight.com/sample-request/hereditary-transthyretin-amyloidosis-hattr-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=ypr

Table of Content
1. Introduction
2. Executive Summary
3. Hereditary Transthyretin Amyloidosis (hATTR): Overview
4. Pipeline Therapeutics
5. Therapeutic Assessment
6. Late Stage Products (Pregistration)
7. Vutrisiran: Alnylam Pharmaceuticals
8. Drug profiles in the detailed report.....
9. Mid Stage Products (Phase II)
10. Drug Name: Company Name
11. Drug profiles in the detailed report.....
12. Early stage products (Phase I)
13. PRX 004: Prothena
14. Drug profiles in the detailed report.....
15. Inactive Products
16. Hereditary Transthyretin Amyloidosis (hATTR) Key Companies
17. Hereditary Transthyretin Amyloidosis (hATTR) Key Products
18. Hereditary Transthyretin Amyloidosis (hATTR)- Unmet Needs
19. Hereditary Transthyretin Amyloidosis (hATTR)- Market Drivers and Barriers
20. Hereditary Transthyretin Amyloidosis (hATTR)- Future Perspectives and Conclusion
21. Hereditary Transthyretin Amyloidosis (hATTR) Analyst Views
22. Hereditary Transthyretin Amyloidosis (hATTR) Key Companies
23. Appendix

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