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Tangram Therapeutics

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uuid0004xi8

Namestring
Tangram Therapeutics
Legal namestring
Tangram Therapeutics
Websiteurl
tangramtx.com
Company typeenum
Private
Founded yearint
2003
Descriptiontext

Tangram Therapeutics is a UK-based clinical-stage biopharmaceutical company developing RNA-interference (RNAi) therapeutics, headquartered in London and operating with 11-50 employees. The company is built around its proprietary GalOmic RNAi drug technology platform, which uses RNA interference to silence disease-causing genes. Its most advanced asset, TGM-312, is a GalOmic RNAi candidate targeting Metabolic dysfunction-Associated SteatoHepatitis (MASH), a progressive liver disease estimated to affect more than 250 million people worldwide. In March 2026, Tangram dosed the first participant in the RESTORE-MASH Phase I/II trial of TGM-312, the first GalOmic candidate from its pipeline to enter clinical-stage testing, with initial safety data expected in H2 2026. A second disclosed candidate, TGM-148, is an oligopeptide inhibitor of matrix metalloproteinase-2 (MMP-2) and MMP-9 being explored for pan-bleeding disorders.

The company is privately held with no parent organization or public listing reported in the inputs. Tangram has raised approximately $148.9M across disclosed rounds between 2009 and 2024, with M&G Investments / M&G Plc and Octopus Ventures among identified investors; a 2016 acquisition of Searchbolt Ltd. brought in additional technology or talent. Leadership comprises Malcolm Young (CEO), Ali Mortazavi (Chairman), Jonny Wray (CTO), Karl Keegan (CFO), and Ankit Sharma (Head of Software Engineering).

Because Tangram has no approved products, its revenue model is anticipated to depend on future one-time licensing and ultimately pharmaceutical product sales through traditional specialty-pharmacy and hospital channels. Currently, the company generates no commercial revenue and is funded entirely by equity capital, with capital deployed against clinical milestones including the ongoing RESTORE-MASH trial and continued advancement of the GalOmic pipeline.

Short descriptiontext

Tangram Therapeutics is a London-based clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics, with lead candidate TGM-312 in a Phase I/II trial for MASH and a second candidate, TGM-148, targeting pan-bleeding disorders.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLondon, United Kingdom
HQ citystring
London
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
RNAi therapeutics, drug discovery, biopharmaceutical development, MASH treatment, RNAi drug platform
Industry3 codes
1RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics)
CodeHLAAADAGPrimaryYes
2RNA Therapeutics Clinical Development (trial design, endpoints, patient stratification)
CodeHLAAADAHPrimaryNo
3Gastroenterology Specialty Pharmaceuticals
CodeHLAIACAEPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
Product category
Clinical-Stage Biopharmaceuticals
Social media profiles2 records
Revenue model1 record
1Pharmaceutical Product Sales
TypeOne Time License
Description

As a clinical-stage biopharmaceutical company, Tangram Therapeutics is in the early development phase with no approved products. Revenue will be generated through future product sales upon successful clinical development and regulatory approval.

globenewswire.com
Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Tangram Therapeutics is a clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics. Its lead asset, TGM-312, is an investigational GalOmic RNAi drug candidate for Metabolic dysfunction-Associated SteatoHepatitis (MASH) currently being evaluated in the RESTORE-MASH Phase I/II trial. The pipeline also includes TGM-148, an oligopeptide inhibitor of MMP-2 and MMP-9 being explored for pan-bleeding disorders.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Phase I/II RESTORE-MASH clinical trial initiated to evaluate safety, pharmacokinetics, and pharmacodynamics in healthy volunteers and MASH patients; initial safety data expected H2 2026
Product overview1 text field

Tangram Therapeutics is a biopharmaceutical company developing RNAi-based therapeutics. The company's product portfolio includes TGM-312, a GalOmic RNAi drug for MASH that recently entered Phase I/II clinical testing, and TGM-148, an oligopeptide inhibitor for pan-bleeding disorders. The company's proprietary GalOmic platform enables the development of RNA interference drugs targeting liver diseases.

Product and service2 records
1TGM-312
CategoryRNAi therapeutic drug candidate
Description

TGM-312 is a GalOmic RNAi drug candidate for treating Metabolic dysfunction-Associated SteatoHepatitis (MASH), a progressive liver disease estimated to affect over 250 million people worldwide with no approved targeted therapies. It is the first GalOmic candidate from Tangram's pipeline to enter clinical-stage testing.

2TGM-148
CategoryOligopeptide therapeutic candidate
Description

TGM-148 is an oligopeptide derivative that acts as an inhibitor for matrix metalloproteinase-2 (MMP-2) and MMP-9, with therapeutic potential for pan-bleeding disorders.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Alnylam is the leading pure-play RNAi therapeutics company with approved products (Onpattro, Givlaari, Oxlumo, Amvuttra) and a broad pipeline including fitusiran for hemophilia. It is the most direct comparable to Tangram's GalOmic RNAi platform given shared modality and liver-directed therapeutic focus.

TypeDirect peer
Description

Arrowhead develops RNAi-based therapeutics using its TRiM platform targeting liver and other tissues, with multiple clinical-stage assets including programs in MASH-adjacent liver disease. It directly mirrors Tangram's strategy of leveraging RNAi to silence disease-causing genes.

TypeDirect peer
Description

Wave is a clinical-stage RNA medicines company developing oligonucleotide-based therapeutics, with multiple programs in metabolic and rare diseases. It is a direct comparable as a small-cap clinical-stage RNA therapeutics player with pipeline breadth.

TypeBroad incumbent
Description

Ionis is the established leader in RNA-targeted therapeutics using antisense oligonucleotides, with dozens of partnered and independent programs. While ASO differs mechanistically from RNAi, the shared goal of RNA-targeted gene silencing for MASH, neurological disease, and bleeding disorders makes it a broad incumbent peer.

TypeDirect peer
Description

Madrigal gained FDA approval for Rezdiffra (resmetirom), the first MASH therapy, and is the most direct commercial reference point for TGM-312. It is a directly comparable MASH-focused therapeutics company competing for the same prescriber and patient pool.

TypeEmerging player
Description

Akero is developing efruxifermin (FGF21 analog) for MASH with two ongoing Phase 3 trials. It is a clinical-stage peer focused on the same indication as Tangram's lead asset, with a differentiated but adjacent mechanism.

TypeEmerging player
Description

Sagimet is a clinical-stage biotech developing denifanstat (FAS inhibitor) for MASH, currently in Phase 3. As another indication-focused MASH competitor, it provides direct comparability on clinical development timelines and capital intensity for Tangram's lead program.

TypeEmerging player
Description

89bio is advancing pegozafermin for MASH in Phase 3 development. As a late-clinical-stage MASH-focused peer, it is a relevant comparable for capital intensity and competitive positioning against TGM-312.

TypeBroad incumbent
Description

Novo Nordisk has positioned semaglutide (Wegovy) for MASH and acquired Dicerna for its RNAi platform. It is a broad incumbent competing in MASH (via GLP-1) and in RNAi (via Dicerna), intersecting directly with Tangram on both axes.

TypeBroad incumbent
Description

Lilly is running Phase 3 trials of tirzepatide in MASH, leveraging its metabolic disease leadership. It is a broad incumbent that competes with RNAi-based approaches via a large, well-capitalized mechanism already established in adjacent metabolic indications.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat2 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds5 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors3 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Tangram Therapeutics

Clinical-Stage Biopharmaceuticalstangramtx.com

Tangram Therapeutics is a London-based clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics, with lead candidate TGM-312 in a Phase I/II trial for MASH and a second candidate, TGM-148, targeting pan-bleeding disorders.

What Tangram Therapeutics does

Tangram Therapeutics is a UK-based clinical-stage biopharmaceutical company developing RNA-interference (RNAi) therapeutics, headquartered in London and operating with 11-50 employees. The company is built around its proprietary GalOmic RNAi drug technology platform, which uses RNA interference to silence disease-causing genes. Its most advanced asset, TGM-312, is a GalOmic RNAi candidate targeting Metabolic dysfunction-Associated SteatoHepatitis (MASH), a progressive liver disease estimated to affect more than 250 million people worldwide. In March 2026, Tangram dosed the first participant in the RESTORE-MASH Phase I/II trial of TGM-312, the first GalOmic candidate from its pipeline to enter clinical-stage testing, with initial safety data expected in H2 2026. A second disclosed candidate, TGM-148, is an oligopeptide inhibitor of matrix metalloproteinase-2 (MMP-2) and MMP-9 being explored for pan-bleeding disorders.

The company is privately held with no parent organization or public listing reported in the inputs. Tangram has raised approximately $148.9M across disclosed rounds between 2009 and 2024, with M&G Investments / M&G Plc and Octopus Ventures among identified investors; a 2016 acquisition of Searchbolt Ltd. brought in additional technology or talent. Leadership comprises Malcolm Young (CEO), Ali Mortazavi (Chairman), Jonny Wray (CTO), Karl Keegan (CFO), and Ankit Sharma (Head of Software Engineering).

Because Tangram has no approved products, its revenue model is anticipated to depend on future one-time licensing and ultimately pharmaceutical product sales through traditional specialty-pharmacy and hospital channels. Currently, the company generates no commercial revenue and is funded entirely by equity capital, with capital deployed against clinical milestones including the ongoing RESTORE-MASH trial and continued advancement of the GalOmic pipeline.

Tangram Therapeutics firmographics

Firmographics
Name
Tangram Therapeutics
Legal name
Tangram Therapeutics
Website
https://tangramtx.com
Company type
Private
Founded year
2003
Operating status
Operating
Headcount range
11–50 employees
Short description
Tangram Therapeutics is a London-based clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics, with lead candidate TGM-312 in a Phase I/II trial for MASH and a second candidate, TGM-148, targeting pan-bleeding disorders.
Ownership category
akta.pro rank

Tangram Therapeutics industry classification

Industry
Product category
Clinical-Stage Biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
akta.pro primary industry
RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics) (HLAAADAG)
akta.pro secondary industries
RNA Therapeutics Clinical Development (trial design, endpoints, patient stratification) (HLAAADAH), Gastroenterology Specialty Pharmaceuticals (HLAIACAE)

Keywords

  • RNAi therapeutics
  • Drug discovery
  • Biopharmaceutical development
  • MASH treatment
  • RNAi drug platform

Where Tangram Therapeutics is headquartered

Location

Headquarters

HQ city
London
HQ country
United Kingdom
HQ region
Europe

Markets served

Tangram Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales

Revenue model

  1. Pharmaceutical Product Sales: As a clinical-stage biopharmaceutical company, Tangram Therapeutics is in the early development phase with no approved products. Revenue will be generated through future product sales upon successful clinical development and regulatory approval.

Tangram Therapeutics product offering

Product offering

Core offering

Tangram Therapeutics is a clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics. Its lead asset, TGM-312, is an investigational GalOmic RNAi drug candidate for Metabolic dysfunction-Associated SteatoHepatitis (MASH) currently being evaluated in the RESTORE-MASH Phase I/II trial. The pipeline also includes TGM-148, an oligopeptide inhibitor of MMP-2 and MMP-9 being explored for pan-bleeding disorders.

Product overview

Tangram Therapeutics is a biopharmaceutical company developing RNAi-based therapeutics. The company's product portfolio includes TGM-312, a GalOmic RNAi drug for MASH that recently entered Phase I/II clinical testing, and TGM-148, an oligopeptide inhibitor for pan-bleeding disorders. The company's proprietary GalOmic platform enables the development of RNA interference drugs targeting liver diseases.

Differentiator

Problem solved

Functional benefit

Products and services

  • TGM-312 TGM-312 is a GalOmic RNAi drug candidate for treating Metabolic dysfunction-Associated SteatoHepatitis (MASH), a progressive liver disease estimated to affect over 250 million people worldwide with no approved targeted therapies. It is the first GalOmic candidate from Tangram's pipeline to enter clinical-stage testing.
  • TGM-148 TGM-148 is an oligopeptide derivative that acts as an inhibitor for matrix metalloproteinase-2 (MMP-2) and MMP-9, with therapeutic potential for pan-bleeding disorders.

Quantifiable outcome

  • Phase I/II RESTORE-MASH clinical trial initiated to evaluate safety, pharmacokinetics, and pharmacodynamics in healthy volunteers and MASH patients; initial safety data expected H2 2026

Companies that use Tangram Therapeutics

Customer profile

Segments2 records

Ideal customer profiles2 records

Tangram Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

Tangram Therapeutics partnerships and signals

Strategic signal

Scale indicators1 record

Recent moves6 records

Expansion highlights5 records

Tangram Therapeutics competitors and assessment

Company assessment

Direct peers

  • Alnylam Pharmaceuticals: Alnylam is the leading pure-play RNAi therapeutics company with approved products (Onpattro, Givlaari, Oxlumo, Amvuttra) and a broad pipeline including fitusiran for hemophilia. It is the most direct comparable to Tangram's GalOmic RNAi platform given shared modality and liver-directed therapeutic focus.
  • Arrowhead Pharmaceuticals: Arrowhead develops RNAi-based therapeutics using its TRiM platform targeting liver and other tissues, with multiple clinical-stage assets including programs in MASH-adjacent liver disease. It directly mirrors Tangram's strategy of leveraging RNAi to silence disease-causing genes.
  • Wave Life Sciences: Wave is a clinical-stage RNA medicines company developing oligonucleotide-based therapeutics, with multiple programs in metabolic and rare diseases. It is a direct comparable as a small-cap clinical-stage RNA therapeutics player with pipeline breadth.
  • Madrigal Pharmaceuticals: Madrigal gained FDA approval for Rezdiffra (resmetirom), the first MASH therapy, and is the most direct commercial reference point for TGM-312. It is a directly comparable MASH-focused therapeutics company competing for the same prescriber and patient pool.

Broad incumbents

  • Ionis Pharmaceuticals: Ionis is the established leader in RNA-targeted therapeutics using antisense oligonucleotides, with dozens of partnered and independent programs. While ASO differs mechanistically from RNAi, the shared goal of RNA-targeted gene silencing for MASH, neurological disease, and bleeding disorders makes it a broad incumbent peer.
  • Novo Nordisk: Novo Nordisk has positioned semaglutide (Wegovy) for MASH and acquired Dicerna for its RNAi platform. It is a broad incumbent competing in MASH (via GLP-1) and in RNAi (via Dicerna), intersecting directly with Tangram on both axes.
  • Eli Lilly: Lilly is running Phase 3 trials of tirzepatide in MASH, leveraging its metabolic disease leadership. It is a broad incumbent that competes with RNAi-based approaches via a large, well-capitalized mechanism already established in adjacent metabolic indications.

Emerging players

  • Akero Therapeutics: Akero is developing efruxifermin (FGF21 analog) for MASH with two ongoing Phase 3 trials. It is a clinical-stage peer focused on the same indication as Tangram's lead asset, with a differentiated but adjacent mechanism.
  • Sagimet Biosciences: Sagimet is a clinical-stage biotech developing denifanstat (FAS inhibitor) for MASH, currently in Phase 3. As another indication-focused MASH competitor, it provides direct comparability on clinical development timelines and capital intensity for Tangram's lead program.
  • 89bio: 89bio is advancing pegozafermin for MASH in Phase 3 development. As a late-clinical-stage MASH-focused peer, it is a relevant comparable for capital intensity and competitive positioning against TGM-312.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat2 records

Key risks6 records

Key highlights6 records

Customer concentration

Tangram Therapeutics social profiles

Digital presence

Tangram Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Tangram Therapeutics leadership team

Management profile

Number of profiles

Profiles5 records

Tangram Therapeutics funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Tangram Therapeutics M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Tangram Therapeutics

What does Tangram Therapeutics do?

Tangram Therapeutics is a clinical-stage biopharmaceutical company developing GalOmic RNAi therapeutics. Its lead asset, TGM-312, is an investigational GalOmic RNAi drug candidate for Metabolic dysfunction-Associated SteatoHepatitis (MASH) currently being evaluated in the RESTORE-MASH Phase I/II trial. The pipeline also includes TGM-148, an oligopeptide inhibitor of MMP-2 and MMP-9 being explored for pan-bleeding disorders.

Is Tangram Therapeutics a public or private company?

Tangram Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Tangram Therapeutics founded?

Tangram Therapeutics was founded in 2003. It employs 11 to 50 people.

Where is Tangram Therapeutics based?

Tangram Therapeutics is headquartered in London, United Kingdom, in the Europe region.

How does Tangram Therapeutics make money?

One revenue line is on record: pharmaceutical Product Sales.

Who are Tangram Therapeutics's main competitors?

Direct peers on record are Alnylam Pharmaceuticals, Arrowhead Pharmaceuticals, Wave Life Sciences and Madrigal Pharmaceuticals. Broad incumbents are Ionis Pharmaceuticals, Novo Nordisk and Eli Lilly. Emerging players are Akero Therapeutics, Sagimet Biosciences and 89bio.

Does Tangram Therapeutics have an API?

No public API is recorded for Tangram Therapeutics.

What industry is Tangram Therapeutics in?

Tangram Therapeutics's product category is Clinical-Stage Biopharmaceuticals. Its primary akta.pro industry code is HLAAADAG, RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics), with a secondary code of HLAAADAH, RNA Therapeutics Clinical Development (trial design, endpoints, patient stratification). Its NAICS code is 541714.

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Live signals
BioWorldPreclinical data support continued development of TGM-148 for bleeding disordersTGM-148, a siRNA developed by Tangram Therapeutics, is designed to repress hepatocyte expression of a gene target to rebalance hemostasis. It has shown efficacy in murine models of hemophilia and von Willebrand disease, supporting continued development for bleeding disorders.GlobeNewswireTangram Therapeutics annonce l’administration de laTangram Therapeutics announced the administration of the first dose to a participant in its RESTORE-MASH Phase I/II clinical trial evaluating TGM-312, a GalOmic RNAi drug for treating Metabolic dysfunction-Associated SteatoHepatitis (MASH), a liver disease estimated to affect over 250 million people worldwide. The trial will assess safety, pharmacokinetics, and pharmacodynamics in healthy volunteers and MASH patients, with initial safety data expected in the second half of 2026. TGM-312 is the first GalOmic drug from Tangram's pipeline to enter clinical-stage testing.GlobeNewswireTangram Therapeutics gibt Dosierung des ersten Studienteilnehmers in der Phase-I/II-Studie RESTORE-MASH zu TGM-312 bekannt, einem in der Entwicklungsphase befindlichen RNAi-TherapeutikumTangram Therapeutics hat die Dosierung des ersten Studienteilnehmers in der Phase-I/II-Studie RESTORE-MASH für TGM-312 bekannt gegeben, ein RNAi-Therapeutikum, das bei MASH-Patienten getestet wird. Die Studie untersucht die Sicherheit, Verträglichkeit, Pharmakokinetik und Pharmakodynamik des Medikaments, mit erwarteten ersten Sicherheitsdaten im zweiten Halbjahr 2026.GlobeNewswireTangram Therapeutics Announces First Participant Dosed in Phase 1/2 RESTORE-MASH Trial of TGM-312, a Novel Investigational RNAi MedicineTangram Therapeutics announced the first participant dosing in its Phase 1/2 RESTORE-MASH trial of TGM-312, a GalOmic RNAi medicine for MASH. The trial evaluates safety, pharmacokinetics, and pharmacodynamics in healthy volunteers and MASH patients, with initial safety data anticipated in H2 2026.GlobeNewswireTangram Therapeutics Submits Clinical Trial Application for Phase 1/2 Study of TGM-312, a Novel Investigational RNAi MASH CandidateTangram Therapeutics submitted a Clinical Trial Application to the UK's Medicines and Healthcare products Regulatory Agency (MHRA) to initiate a Phase 1/2 clinical trial of its lead pipeline candidate TGM-312, a GalOmic siRNA therapeutic designed to treat metabolic dysfunction-associated steatohepatitis (MASH). The first-in-human study is expected to commence in early 2026 in the United Kingdom, with initial data anticipated in H2 2026. This milestone marks Tangram's transition into a clinical-stage company, advancing its first GalOmic medicine from discovery into clinical development.BioSpaceTangram Therapeutics Submits Clinical Trial Application for Phase 1/2 Study of TGM-312, a Novel Investigational RNAi MASH CandidateTangram Therapeutics announced the submission of a Clinical Trial Application to the UK's Medicines and Healthcare products Regulatory Agency (MHRA) to initiate a Phase 1/2 clinical trial of its lead pipeline program TGM-312, an investigational GalOmic siRNA designed to silence a novel hepatocyte gene for treating metabolic dysfunction-associated steatohepatitis (MASH). Pending regulatory clearance, the first-in-human study is expected to commence in early 2026 in the United Kingdom, with initial data anticipated in H2 2026. The milestone marks Tangram's advancement into clinical-stage development as its first GalOmic medicine enters the clinic.GlobeNewswiree-therapeutics Relaunches as Tangram Therapeutics and Unveils LLibra OSTangram Therapeutics, formerly e-therapeutics, relaunched and unveiled LLibra OS, an AI platform for RNAi drug discovery. Its lead program TGM-312 for MASH is on track for a CTA submission in Q4 2025, with TGM-148 for bleeding disorders planned for 2026.