Shape Therapeutics

Shape Therapeutics

AI-driven RNA medicine discovery platform

Overview

Shape Therapeutics uses AI to design RNA-based medicines that reprogram cells to prevent or treat disease, analyzing large genomic datasets to find new treatment possibilities. Its platform designs RNAs and uses RNAfix to recode RNA with a natural cellular enzyme, correcting protein-coding instructions without changing DNA, and it tailors gene expression with smart-sensing vector designs while engineering billions of viral capsids for tissue-specific RNA delivery. Unlike traditional gene therapies, ShapeTX combines AI-driven RNA design, RNA-level edits, and targeted delivery to enable new treatment possibilities beyond first-generation approaches. The goal is to discover medicines that address the root causes of diseases while prioritizing safety, manufacturability, and precise tissue targeting.

About Shape Therapeutics

Simplify's Rating
Why Shape Therapeutics is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Data & Analytics

AI & Machine Learning

Biotechnology

Healthcare

Company Size

11-50

Company Stage

Series B

Total Funding

$147.5M

Headquarters

Seattle, Washington

Founded

2018

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Simplify's Take

What believers are saying

  • MJFF funded SHP-201 on July 29, 2026, advancing IND-enabling Parkinson’s work.
  • RSRT partnered on August 6, 2026 to advance SHP-401 for Rett syndrome.
  • VectorY’s September 18, 2025 deal priced Shape’s capsid at up to $1.2 billion.

What critics are saying

  • June 2025 brought an interim-CEO transition, signaling leadership instability at ShapeTX.
  • BioSpace reported layoffs in early 2026, forcing a pipeline-only reset and cash preservation.
  • If SHP-201 and SHP-401 miss IND milestones, ShapeTX becomes a stranded platform.

What makes Shape Therapeutics unique

  • ShapeTX owns SHP-DB1, an AAV5-derived CNS capsid licensed to VectorY in September 2025.
  • Its RNAfix platform edits RNA without permanent DNA changes, spanning Rett and Parkinson’s.
  • The company pairs AI-designed payloads with delivery technology, not a single-asset program.

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Funding

Total Funding

$147.5M

Above

Industry Average

Funded Over

2 Rounds

Series B funding is typically for startups that have proven their business model and need more funding to expand rapidly—often by entering new markets or adding more products. Investors are usually venture capital firms that specialize in later-stage investments.
Series B Funding Comparison
Above Average

Industry standards

$35M
$45M
Linktree
$65M
Substack
$100M
ClickUp
$112M
Shape Therapeutics

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Paid Holidays

Parental Leave

Unlimited Paid Time Off

Disability Insurance

401(k) Retirement Plan

Life Insurance

Health Savings Account/Flexible Spending Account

Growth & Insights and Company News

Headcount

6 month growth

-8%

1 year growth

-15%

2 year growth

0%
Associated Press
Jul 29th, 2026
Shape Therapeutics gets MJFF grant to advance SHP-201 gene therapy for Parkinson's disease

Shape Therapeutics has received a research grant from The Michael J. Fox Foundation for Parkinson's Research to advance SHP-201, a one-time gene therapy for Parkinson's disease. The grant will support preclinical studies examining the pharmacology, pharmacokinetics, and safety of SHP-201 ahead of an investigational new drug submission for clinical trials. SHP-201 combines Shape's blood-brain barrier-crossing AAV capsid with an RNA-editing payload that targets the SNCA transcript to reduce alpha-synuclein protein production. The therapy is designed to be delivered as a single intravenous infusion, providing durable brain-wide alpha-synuclein reduction. The grant was awarded through the foundation's Parkinson's Disease Therapeutics Pipeline Program, which supports preclinical and translational research for promising therapeutic approaches.

GlobeNewswire
Jul 29th, 2026
Shape Therapeutics Receives Research Grant from The Michael J. Fox Foundation for Parkinson’s Research to Advance SHP-201, a One-Time Gene Therapy to Treat Parkinson’s Disease

Grant supports IND-enabling studies of an intravenously delivered, disease-modifying gene therapy designed to reduce alpha-synuclein in the brain regions...

DealForma
Dec 16th, 2025
Neurology R&D Partnerships, M&A and Venture Funding - Q3 2025 Review

Neurology R&D Partnerships, M&A and Venture Funding - Q3 2025 review. Its review of the Q3 2025 neurology activity shows a mixed but broadly active market. R&D partnerships gained momentum, with 23 deals totaling $9.2 billion, driven by larger or more incentive-rich agreements. Upfront payments remained stable, while total deal value growth suggests sponsors are structuring partnerships with long-term milestones. Notable R&D deals include Arrowhead - Novartis ($200 million upfront, $2 billion potential milestones), Merck - Skyhawk (>$2 billion potential), and VectorY - Shape ($359 million upfront/option payments, up to $1.2 billion total). M&A activity softened, with 18 deals worth $1.9 billion and lower cash outlays, indicating increased reliance on contingent payments and earnouts. In contrast, Q2 saw stronger upfront commitments. Major transactions included AbbVie's $1.2 billion acquisition of Gilgamesh Pharmaceuticals, Remedy Meds' $500+ million all-stock purchase of Thirty Madison, and the NeuroX - Relief Therapeutics merger ($1.2 billion NeuroX valuation). Venture Funding, moderated, with 35 rounds raising $1.3 billion versus $1.9 billion in Q2. Investment remained concentrated in select high-potential programs, including MapLight Therapeutics' $373 million series D, Imagine Pediatrics' $67 million series B, and NRG Therapeutics' $67 million series B. Overall, the sector demonstrated strong R&D activity with significant long-term value creation, experienced cautious M&A characterized by lower upfront cash and saw selective venture funding. Neurology R&D Partnerships Neurology R&D partnering accelerated in Q3 2025, with 23 deals totaling $9.2 billion and $294 million in upfront payments. A modest increase in volume and a significant rise in total deal value compared with Q2, pointing to larger or more incentive-rich structures even as upfront spending stayed stable. Q2 recorded 17 partnerships worth $6.4 billion with $254 million upfront, showing that while fewer deals closed, sponsors maintained consistent near-term capital deployment and concentrated variability in longer-term milestones. Across Q2 and Q3 combined, neurology partnerships reached 40 deals and $15.6 billion in value, with $548 million upfront. Top Neurology R&D Partnership in Q3 2025 Arrowhead granted Novartis exclusive global rights to ARO SNCA, a preclinical siRNA therapy targeting alpha synuclein for Parkinson's disease and other synucleinopathies. The collaboration leverages Arrowhead's TRiM RNAi platform, with Novartis also holding an option to add additional TRiM-based targets. Arrowhead will complete all CTA enabling preclinical work, after which Novartis will take over clinical development, manufacturing, medical affairs, and commercialization. Financial terms include a $200-million upfront payment and up to $2 billion in potential development, regulatory, and sales milestones, along with tiered royalties. Merck entered a research partnership with Skyhawk Therapeutics to identify RNA-targeting small molecules for neurological disorders using Skyhawk's SkySTAR platform. Skyhawk will lead discovery and preclinical activities, while Merck holds an exclusive global option to advance and commercialize any resulting therapies. If Merck exercises this option, it will take on all further development and commercialization. Skyhawk is eligible for more than $2 billion in upfront and milestone payments, along with tiered royalties. VectorY Therapeutics partnered with Shape Therapeutics to develop vectorized antibody therapies for three neurodegenerative programs using Shape's engineered AAV5-derived SHP-DB1 capsid, designed for deep-brain penetration and reduced toxicity. VectorY holds an option to develop and commercialize resulting therapies, supporting IV delivery for ALS, Huntington's, and Alzheimer's. Financial terms include an undisclosed upfront and option payments totaling $359 million, with Shape eligible for up to $1.2 billion in total deal value, including $338 million in milestones for rare disease programs, $504 million for non-rare programs, plus tiered royalties. Neurology M&A Neurology M&A activity softened in Q3 2025, with 18 deals valued at $1.9 billion, including contingents, and only $710 million paid in cash. This reflects both smaller transactions and a heavier use of earnouts, which accounted for about $1.2 billion of the total. By comparison, Q2 was materially stronger with 24 deals totaling $3 billion and $2.5 billion in cash consideration, indicating buyers were more willing to commit upfront and with greater certainty. Taken together, Q2 and Q3 delivered 42 deals worth $4.9 billion and $3.2 billion in cash. Top Neurology M&A in Q3 2025 AbbVie acquired Gilgamesh Pharmaceuticals to secure Bretisilocin, a Phase II 5-HT2A receptor agonist and 5-HT releaser for major depressive disorder. Gilgamesh spun off its other programs, including blixeprodil and the cardio-safe ibogaine analog M1/M4 agonist program, into a new entity, Gilgamesh Pharma, Inc., which will continue development of existing collaborations with AbbVie. Financial terms include up to $1.2 billion in total consideration, covering upfront and development milestones. The acquisition was completed on October 17, 2025. Remedy Meds is acquiring Thirty Madison in an all-stock transaction. Thirty Madison delivers telehealth-based, personalized care for chronic conditions, combining virtual consultations, customized treatments, and home delivery. The acquisition will expand Remedy Meds' telehealth platform, integrating Thirty Madison's brands to broaden access, accelerate treatment, and enhance operational scale across men's, women's, and metabolic health. The deal, expected to close in Q4 2025, values Thirty Madison at over $500 million upfront. NeuroX is reverse merging with Relief Therapeutics to secure a public listing on the SIX Swiss Exchange. The combined company will focus on digital therapies for neurological disorders, integrating NeuroX's AI platform and MindMaze product portfolio with Relief's market services. Upon completion, NeuroX shareholders will hold 91% of the merged entity, and Relief shareholders 9%, based on valuations of CHF 1 billion ($1.2 billion) for NeuroX and CHF 100 million ($125 million) for Relief. The merger, expected to close in Q4 2025, was approved by Relief shareholders on November 17, 2025, creating MindMaze Therapeutics Holding SA. The transaction includes issuing 140 million new shares, restructuring capital, and appointing a leadership team from NeuroX and MindMaze. On December 15, 2025, the business combination between MindMaze and NeuroX was completed. The newly combined entity now operates under the name MindMaze Therapeutics Holding SA. Neurology Venture Funding Activity Neurology venture funding moderated in Q3 2025, with 35 rounds totaling $1.3 billion, reflecting both fewer financings and lower capital deployment than the prior quarter. Q2 was notably stronger, with 41 rounds raising $1.9 billion, signaling a more risk-on environment and the presence of several larger rounds that boosted aggregate funding. Across Q2 and Q3, the sector recorded 76 rounds and $3 billion. Top Neurology Venture Funding in Q3 2025 MapLight Therapeutics announced an oversubscribed $373 million series D financing co-led by Forbion and Life Sciences at Goldman Sachs Alternatives, with participation from new investors including Sanofi, T. Rowe Price-advised accounts, and Avego BioScience Capital, as well as existing backers such as Novo Holdings, 5AM Ventures, and Blue Owl Healthcare Opportunities. The funding will advance MapLight's lead program, ML-007C-MA, an oral fixed-dose combination of the M1/M4 muscarinic agonist ML-007 with a peripherally acting anticholinergic, designed to enhance CNS efficacy while reducing peripheral side effects. Proceeds will support ongoing Phase 2 trials in schizophrenia and Alzheimer's disease psychosis, exploration of additional indications, and the continued development of other clinical and preclinical pipeline programs. MapLight is a clinical-stage biopharmaceutical company focused on CNS disorders. Imagine Pediatrics, a tech-enabled pediatric medical group providing 24/7 virtual and in-home care for children with special health care needs, has raised $67 million in series B funding. Existing investors Oak HC/FT, Optum Ventures, and Rubicon Founders participated, alongside new strategic investment from the Autism Impact Fund and others. Founded in 2022, Imagine Pediatrics serves roughly 40,000 children nationwide through an integrated medical, behavioral, and social care model. The funding will support national expansion, enhance the company's proprietary technology platform, and drive clinical innovation to close care gaps and improve access to specialized pediatric services under value-based care arrangements. NRG Therapeutics closed an oversubscribed £50 million ($67 million) series B to advance Parkinson's studies and achieve proof of concept in ALS/MND. Led by SV Health Investors' Dementia Discovery Fund, the round included British Business Bank, M Ventures, Novartis Venture Fund, Criteria Bio Ventures, and existing investors Omega Funds and Brandon Capital. The financing will support Phase 1b Parkinson's trials and ALS/MND development of NRG5051, a first-in-class oral mPTP inhibitor targeting mitochondrial dysfunction and neuronal death, with potential to expand across other neurodegenerative indications.

PharmaShots
Sep 18th, 2025
VectorY Therapeutics Collaborates with Shape Therapeutics to Develop Vectorized Antibodies for Neurodegenerative Diseases

VectorY Therapeutics collaborates with Shape Therapeutics to develop vectorized antibodies for neurodegenerative diseases.

Pharma Focus America
Oct 4th, 2024
Shape Therapeutics Unveils Major Advances in AI-Powered Platform for Precision RNA Editing

Shape Therapeutics, a leader in RNA-based gene therapy, today released two preprint manuscripts detailing major technological breakthroughs that underpin the company's therapeutic editing platform RNAfix(R).

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