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Triana Biomedicines

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uuid0000l5w

Namestring
Triana Biomedicines
Legal namestring
Triana Biomedicines, Inc.
Websiteurl
trianabio.com
Company typeenum
Private
Founded yearint
2021
Descriptiontext

Triana Biomedicines is a venture-backed, clinical-stage biopharmaceutical company developing targeted protein degradation (TPD) therapies through a proprietary molecular glue discovery platform. Founded in 2021 and headquartered in Lexington, Massachusetts, the company applies a target-first and rational approach that evaluates over 600 known E3 ubiquitin ligases against disease-relevant targets, using a protein:protein pairing engine, high-resolution structural insights, AI/computational tools, and bespoke chemical libraries to identify small molecules that promote protein-protein interactions and selectively degrade disease-causing proteins. Its stated focus is the approximately 85% of disease targets considered undruggable by traditional small-molecule or biologic modalities.

The company's pipeline is led by TRI-611, an oral, brain-penetrant, molecular glue degrader that targets ALK fusion proteins in ALK-positive non-small cell lung cancer (ALK+ NSCLC) through a mechanism independent of the ALK kinase active site, designed to overcome resistance to existing tyrosine kinase inhibitors. TRI-611 entered a global Phase 1/2 first-in-human trial in March 2026 and received U.S. FDA Fast Track designation the same month for patients who have failed two or more ALK TKIs. A second program targets cyclin E1 (CCNE1) for CCNE1-amplified tumors and a subset of HR+/HER2- breast cancers and remains preclinical.

Triana operates a capital- and collaboration-driven business model. The company is pre-revenue on a product basis and instead earns upfront payments, milestone payments, and royalties through strategic research collaborations and licensing agreements with large pharmaceutical partners, notably Pfizer ($49 million upfront plus potential milestones exceeding $1.5 billion and tiered royalties, signed October 2024) and Johnson & Johnson (research collaboration signed January 2026). Since inception Triana has raised approximately $279 million across seed, Series A ($110 million in April 2022), Series B ($120 million in December 2025), and the Pfizer upfront, with a top-tier investor syndicate including RA Capital, Atlas Venture, Lightspeed Venture Partners, Pfizer Ventures, Ascenta Capital, and Bessemer Venture Partners. The company plans to advance proprietary assets toward proof-of-concept and to pursue either partnership-based or independent commercialization for approved products.

Short descriptiontext

Triana Biomedicines is a clinical-stage biopharmaceutical company developing molecular glue degraders that selectively eliminate disease-causing proteins, with lead asset TRI-611 in Phase 1/2 trials for ALK-positive NSCLC and additional programs targeting CCNE1-amplified tumors, serving patients with cancers resistant to existing therapies.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLexington, United States
HQ citystring
Lexington
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
molecular glue discovery, targeted protein degradation, cancer therapeutics development, E3 ligase platform, biopharmaceutical research
Industry2 codes
1Protein Interaction & Structural Biology Platforms (cryo-EM, X-ray, NMR, biophysics)
CodeHLAAAIAHPrimaryYes
2Target Identification & Validation Platforms (omics-driven, chemoproteomics, genetic validation)
CodeHLAAAIAIPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Targeted Protein Degradation Therapeutics
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Strategic collaborations and licensing (milestone and royalty payments)
TypeLicensing Royalties
Description

TRIANA earns upfront payments, milestone payments, and royalties through strategic research collaborations and licensing agreements with pharmaceutical partners. The Pfizer collaboration includes a $49 million upfront payment with potential future milestone payments exceeding $1.5 billion plus tiered royalties. This represents a primary revenue model for the company as a platform-focused biotech.

trianabio.com
2Upfront collaboration payments
TypeOne Time License
trianabio.com
3Future product commercialization
TypeLicensing Royalties
trianabio.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Personnel, Technology or R&D, Operations, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Triana Biomedicines operates a target-first molecular glue discovery platform that systematically identifies small molecules promoting protein-protein interactions to harness the cell's ubiquitin-proteasome system for targeted protein degradation. The company develops proprietary drug candidates including TRI-611 (oral, brain-penetrant ALK degrader for ALK+ NSCLC in Phase 1/2) and a CCNE1 degrader program for cyclin E1-amplified tumors. Revenue is generated through pharmaceutical licensing collaborations and milestone/royalty arrangements with major pharma partners.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • TRI-611 received FDA Fast Track designation for ALK+ NSCLC patients who have failed two or more ALK TKIs (March 2026)
+3 more records
Product overview1 text field

Triana Biomedicines is a venture-backed biopharmaceutical company operating a target-first and rational molecular glue discovery platform. The platform identifies small molecules that promote interactions between disease-causing proteins and components of the cell's ubiquitin-proteasome system (E3 ligases), enabling targeted protein degradation of traditionally undruggable disease targets. The current pipeline consists of TRI-611 (lead clinical-stage ALK-targeted molecular glue degrader for ALK+ non-small cell lung cancer in Phase 1/2) and CCNE1 (preclinical cyclin E1 degrader for CCNE1-amplified tumors and HR+/HER2- breast cancer). The company leverages proprietary protein:protein pairing engines, bespoke chemical libraries, and AI/computational tools in its drug discovery efforts.

Product and service3 records
1TRI-611
CategoryOncology Therapeutics / Molecular Glue Degrader
Description

Novel oral, small-molecule molecular glue degrader designed to target and degrade ALK fusion proteins in patients with ALK-positive non-small cell lung cancer. Brings ALK and cereblon together through a unique binding mechanism independent of the kinase active site, harnessing the body's innate protein-degradation machinery to selectively eliminate the ALK fusion protein. Brain-penetrant and designed for patients who have failed two or more ALK tyrosine kinase inhibitors. Currently in Phase 1/2 clinical trial.

2CCNE1 Program
CategoryOncology Therapeutics / Molecular Glue Degrader
Description

Preclinical molecular glue degrader program targeting cyclin E1 (CCNE1) for the treatment of CCNE1-amplified tumors and a subset of HR+/HER2- breast cancers. Harnesses the cell's protein degradation machinery to substantially decrease excess CCNE1 and halt growth of CCNE1-dependent tumor cells. Designed to address limited treatment options for CCNE1-amplified tumors and resistance to CDK4/6 inhibitors in HR+/HER2- breast cancer.

3Molecular Glue Discovery Platform
CategoryDrug Discovery Platform / Technology
Description

Target-first and rational molecular glue discovery platform that evaluates and prioritizes over 600 known E3 ubiquitin ligases and their disease-relevant targets. Powered by high-resolution structural insights, state-of-the-art AI and computational tools, and bespoke chemical libraries to identify small molecules promoting protein-protein interactions for targeted protein degradation. Licensed to pharmaceutical partners (Pfizer, Johnson & Johnson) for molecular glue discovery collaborations.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-06
Description

TRIANA entered into a research collaboration with Johnson & Johnson to advance the discovery of important molecular glue targets in oncology. The collaboration applies TRIANA's proprietary molecular glue discovery platform to targets that have been inadequately targeted or considered undruggable.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-10-15
Description

TRIANA entered into a strategic collaboration and licensing agreement with Pfizer to discover novel molecular glue degraders for multiple targets across various disease areas including oncology. TRIANA received a $49 million upfront payment and is eligible for potential future milestone payments exceeding $1.5 billion plus tiered royalties. TRIANA leads discovery and identification of development candidates; Pfizer has exclusive option for exclusive license to pursue further preclinical and clinical development.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Pioneer in targeted protein degradation using PROTACs and molecular glues, with clinical-stage oncology assets (ARV-471, ARV-110). Directly comparable as a TPD-focused biotech with a similar platform approach to tackling previously undruggable targets in oncology.

TypeDirect peer
Description

Clinical-stage biotech developing targeted protein degraders with a proprietary Pegasus discovery platform. Directly comparable to Triana's molecular glue approach, with multiple programs in oncology and immunology and major pharma partnerships (Vertex, Sanofi).

TypeDirect peer
Description

Clinical-stage biotech focused on molecular glue degraders for cancer and other diseases, with lead assets targeting GSPT1 and NEK7. Direct competitor in molecular glue discovery with a similar platform-based approach and Novartis collaboration.

TypeDirect peer
Description

Clinical-stage biotech developing small molecule degraders including the TORPEDO platform for targeted protein degradation. Direct competitor with clinical-stage assets in oncology and partnerships with major pharma including Biogen and Roche.

TypeDirect peer
Description

Clinical-stage biotech developing targeted protein degradation therapies using ligase modulators. Direct competitor with DELigase platform and clinical assets including NX-2127 and NX-5948, plus major pharma partnerships with Gilead, Pfizer, and Sanofi.

TypeDirect peer
Description

Private biotech developing cell-penetrating miniproteins (CPMPs) for cancer, with a platform approach to challenging undruggable targets. Comparable as a platform-based oncology company tackling similar target classes where Triana's VP of Medicinal Chemistry previously served as Head of Medicinal Chemistry.

TypeDirect peer
Description

Private biotech developing next-generation targeted protein degradation therapies with a focus on novel mechanisms beyond cereblon. Comparable platform-based TPD approach with a major pharma partnership with Bristol Myers Squibb valued at over $2B.

TypeDirect peer
Description

Private biotech focused on discovering molecular glue degraders for undruggable targets in oncology and other diseases. Direct competitor with an AbbVie partnership for molecular glue discovery and significant venture backing from Bain Capital Life Sciences.

TypeEmerging player
Description

Private biotech developing LYTACs (lysosomal targeting chimeras) for extracellular protein degradation. Adjacent technology platform addressing the similar undruggable target opportunity through a different mechanism, with backing from founding investor Versant Ventures.

TypeBroad incumbent
Description

Large pharmaceutical company with major targeted protein degradation efforts, including a $2B+ partnership with Amphista Therapeutics and active internal TPD research programs. Operates broadly across oncology including protein degradation research and is a potential strategic acquirer of platform-based TPD companies.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 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

Investors12 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&A

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 →

Triana Biomedicines

Targeted Protein Degradation Therapeuticstrianabio.com

Triana Biomedicines is a clinical-stage biopharmaceutical company developing molecular glue degraders that selectively eliminate disease-causing proteins, with lead asset TRI-611 in Phase 1/2 trials for ALK-positive NSCLC and additional programs targeting CCNE1-amplified tumors, serving patients with cancers resistant to existing therapies.

What Triana Biomedicines does

Triana Biomedicines is a venture-backed, clinical-stage biopharmaceutical company developing targeted protein degradation (TPD) therapies through a proprietary molecular glue discovery platform. Founded in 2021 and headquartered in Lexington, Massachusetts, the company applies a target-first and rational approach that evaluates over 600 known E3 ubiquitin ligases against disease-relevant targets, using a protein:protein pairing engine, high-resolution structural insights, AI/computational tools, and bespoke chemical libraries to identify small molecules that promote protein-protein interactions and selectively degrade disease-causing proteins. Its stated focus is the approximately 85% of disease targets considered undruggable by traditional small-molecule or biologic modalities.

The company's pipeline is led by TRI-611, an oral, brain-penetrant, molecular glue degrader that targets ALK fusion proteins in ALK-positive non-small cell lung cancer (ALK+ NSCLC) through a mechanism independent of the ALK kinase active site, designed to overcome resistance to existing tyrosine kinase inhibitors. TRI-611 entered a global Phase 1/2 first-in-human trial in March 2026 and received U.S. FDA Fast Track designation the same month for patients who have failed two or more ALK TKIs. A second program targets cyclin E1 (CCNE1) for CCNE1-amplified tumors and a subset of HR+/HER2- breast cancers and remains preclinical.

Triana operates a capital- and collaboration-driven business model. The company is pre-revenue on a product basis and instead earns upfront payments, milestone payments, and royalties through strategic research collaborations and licensing agreements with large pharmaceutical partners, notably Pfizer ($49 million upfront plus potential milestones exceeding $1.5 billion and tiered royalties, signed October 2024) and Johnson & Johnson (research collaboration signed January 2026). Since inception Triana has raised approximately $279 million across seed, Series A ($110 million in April 2022), Series B ($120 million in December 2025), and the Pfizer upfront, with a top-tier investor syndicate including RA Capital, Atlas Venture, Lightspeed Venture Partners, Pfizer Ventures, Ascenta Capital, and Bessemer Venture Partners. The company plans to advance proprietary assets toward proof-of-concept and to pursue either partnership-based or independent commercialization for approved products.

Triana Biomedicines firmographics

Firmographics
Name
Triana Biomedicines
Legal name
Triana Biomedicines, Inc.
Website
https://trianabio.com
Company type
Private
Founded year
2021
Operating status
Operating
Headcount range
11–50 employees
Short description
Triana Biomedicines is a clinical-stage biopharmaceutical company developing molecular glue degraders that selectively eliminate disease-causing proteins, with lead asset TRI-611 in Phase 1/2 trials for ALK-positive NSCLC and additional programs targeting CCNE1-amplified tumors, serving patients with cancers resistant to existing therapies.
Ownership category
akta.pro rank

Triana Biomedicines industry classification

Industry
Product category
Targeted Protein Degradation Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Protein Interaction & Structural Biology Platforms (cryo-EM, X-ray, NMR, biophysics) (HLAAAIAH)
akta.pro secondary industry
Target Identification & Validation Platforms (omics-driven, chemoproteomics, genetic validation) (HLAAAIAI)

Keywords

  • Molecular glue discovery
  • Targeted protein degradation
  • Cancer therapeutics development
  • E3 ligase platform
  • Biopharmaceutical research

Where Triana Biomedicines is headquartered

Location

Headquarters

HQ city
Lexington
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Triana Biomedicines business model

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

Revenue model

  1. Strategic collaborations and licensing (milestone and royalty payments): TRIANA earns upfront payments, milestone payments, and royalties through strategic research collaborations and licensing agreements with pharmaceutical partners. The Pfizer collaboration includes a $49 million upfront payment with potential future milestone payments exceeding $1.5 billion plus tiered royalties. This represents a primary revenue model for the company as a platform-focused biotech.
  2. Upfront collaboration payments:
  3. Future product commercialization:

Go-to-market motion1 record

Distribution channels2 records

Marketing channels5 records

Triana Biomedicines product offering

Product offering

Core offering

Triana Biomedicines operates a target-first molecular glue discovery platform that systematically identifies small molecules promoting protein-protein interactions to harness the cell's ubiquitin-proteasome system for targeted protein degradation. The company develops proprietary drug candidates including TRI-611 (oral, brain-penetrant ALK degrader for ALK+ NSCLC in Phase 1/2) and a CCNE1 degrader program for cyclin E1-amplified tumors. Revenue is generated through pharmaceutical licensing collaborations and milestone/royalty arrangements with major pharma partners.

Product overview

Triana Biomedicines is a venture-backed biopharmaceutical company operating a target-first and rational molecular glue discovery platform. The platform identifies small molecules that promote interactions between disease-causing proteins and components of the cell's ubiquitin-proteasome system (E3 ligases), enabling targeted protein degradation of traditionally undruggable disease targets. The current pipeline consists of TRI-611 (lead clinical-stage ALK-targeted molecular glue degrader for ALK+ non-small cell lung cancer in Phase 1/2) and CCNE1 (preclinical cyclin E1 degrader for CCNE1-amplified tumors and HR+/HER2- breast cancer). The company leverages proprietary protein:protein pairing engines, bespoke chemical libraries, and AI/computational tools in its drug discovery efforts.

Differentiator

Problem solved

Functional benefit

Products and services

  • TRI-611 Novel oral, small-molecule molecular glue degrader designed to target and degrade ALK fusion proteins in patients with ALK-positive non-small cell lung cancer. Brings ALK and cereblon together through a unique binding mechanism independent of the kinase active site, harnessing the body's innate protein-degradation machinery to selectively eliminate the ALK fusion protein. Brain-penetrant and designed for patients who have failed two or more ALK tyrosine kinase inhibitors. Currently in Phase 1/2 clinical trial.
  • CCNE1 Program Preclinical molecular glue degrader program targeting cyclin E1 (CCNE1) for the treatment of CCNE1-amplified tumors and a subset of HR+/HER2- breast cancers. Harnesses the cell's protein degradation machinery to substantially decrease excess CCNE1 and halt growth of CCNE1-dependent tumor cells. Designed to address limited treatment options for CCNE1-amplified tumors and resistance to CDK4/6 inhibitors in HR+/HER2- breast cancer.
  • Molecular Glue Discovery Platform Target-first and rational molecular glue discovery platform that evaluates and prioritizes over 600 known E3 ubiquitin ligases and their disease-relevant targets. Powered by high-resolution structural insights, state-of-the-art AI and computational tools, and bespoke chemical libraries to identify small molecules promoting protein-protein interactions for targeted protein degradation. Licensed to pharmaceutical partners (Pfizer, Johnson & Johnson) for molecular glue discovery collaborations.

Quantifiable outcome

  • TRI-611 received FDA Fast Track designation for ALK+ NSCLC patients who have failed two or more ALK TKIs (March 2026)
  • +3 more outcomes

Companies that use Triana Biomedicines

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

Triana Biomedicines technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Triana Biomedicines partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • Johnson & Johnson (Janssen Pharmaceutica NV)coreStrategic or Co-development Partner · 6 January 2026TRIANA entered into a research collaboration with Johnson & Johnson to advance the discovery of important molecular glue targets in oncology. The collaboration applies TRIANA's proprietary molecular glue discovery platform to targets that have been inadequately targeted or considered undruggable.
  • PfizercoreStrategic or Co-development Partner · 15 October 2024TRIANA entered into a strategic collaboration and licensing agreement with Pfizer to discover novel molecular glue degraders for multiple targets across various disease areas including oncology. TRIANA received a $49 million upfront payment and is eligible for potential future milestone payments exceeding $1.5 billion plus tiered royalties. TRIANA leads discovery and identification of development candidates; Pfizer has exclusive option for exclusive license to pursue further preclinical and clinical development.

Scale indicators10 records

Recent moves6 records

Expansion highlights6 records

Triana Biomedicines competitors and assessment

Company assessment

Direct peers

  • Arvinas: Pioneer in targeted protein degradation using PROTACs and molecular glues, with clinical-stage oncology assets (ARV-471, ARV-110). Directly comparable as a TPD-focused biotech with a similar platform approach to tackling previously undruggable targets in oncology.
  • Kymera Therapeutics: Clinical-stage biotech developing targeted protein degraders with a proprietary Pegasus discovery platform. Directly comparable to Triana's molecular glue approach, with multiple programs in oncology and immunology and major pharma partnerships (Vertex, Sanofi).
  • Monte Rosa Therapeutics: Clinical-stage biotech focused on molecular glue degraders for cancer and other diseases, with lead assets targeting GSPT1 and NEK7. Direct competitor in molecular glue discovery with a similar platform-based approach and Novartis collaboration.
  • C4 Therapeutics: Clinical-stage biotech developing small molecule degraders including the TORPEDO platform for targeted protein degradation. Direct competitor with clinical-stage assets in oncology and partnerships with major pharma including Biogen and Roche.
  • Nurix Therapeutics: Clinical-stage biotech developing targeted protein degradation therapies using ligase modulators. Direct competitor with DELigase platform and clinical assets including NX-2127 and NX-5948, plus major pharma partnerships with Gilead, Pfizer, and Sanofi.
  • Fog Pharma: Private biotech developing cell-penetrating miniproteins (CPMPs) for cancer, with a platform approach to challenging undruggable targets. Comparable as a platform-based oncology company tackling similar target classes where Triana's VP of Medicinal Chemistry previously served as Head of Medicinal Chemistry.
  • Amphista Therapeutics: Private biotech developing next-generation targeted protein degradation therapies with a focus on novel mechanisms beyond cereblon. Comparable platform-based TPD approach with a major pharma partnership with Bristol Myers Squibb valued at over $2B.
  • Neomorph: Private biotech focused on discovering molecular glue degraders for undruggable targets in oncology and other diseases. Direct competitor with an AbbVie partnership for molecular glue discovery and significant venture backing from Bain Capital Life Sciences.

Emerging players

  • Lycia Therapeutics: Private biotech developing LYTACs (lysosomal targeting chimeras) for extracellular protein degradation. Adjacent technology platform addressing the similar undruggable target opportunity through a different mechanism, with backing from founding investor Versant Ventures.

Broad incumbents

  • Bristol Myers Squibb: Large pharmaceutical company with major targeted protein degradation efforts, including a $2B+ partnership with Amphista Therapeutics and active internal TPD research programs. Operates broadly across oncology including protein degradation research and is a potential strategic acquirer of platform-based TPD companies.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks5 records

Key highlights6 records

Customer concentration

Triana Biomedicines social profiles

Digital presence

Triana Biomedicines financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Triana Biomedicines leadership team

Management profile

Number of profiles

Profiles11 records

Triana Biomedicines funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors12 records

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

Triana Biomedicines M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Triana Biomedicines

What does Triana Biomedicines do?

Triana Biomedicines operates a target-first molecular glue discovery platform that systematically identifies small molecules promoting protein-protein interactions to harness the cell's ubiquitin-proteasome system for targeted protein degradation. The company develops proprietary drug candidates including TRI-611 (oral, brain-penetrant ALK degrader for ALK+ NSCLC in Phase 1/2) and a CCNE1 degrader program for cyclin E1-amplified tumors. Revenue is generated through pharmaceutical licensing collaborations and milestone/royalty arrangements with major pharma partners.

Is Triana Biomedicines a public or private company?

Triana Biomedicines is a private company. It is classified as venture growth investor backed and is currently operating.

When was Triana Biomedicines founded?

Triana Biomedicines was founded in 2021. It employs 11 to 50 people.

Where is Triana Biomedicines based?

Triana Biomedicines is headquartered in Lexington, United States, in the North America region.

How does Triana Biomedicines make money?

Three revenue lines are on record. Strategic collaborations and licensing (milestone and royalty payments) is the primary driver. The others are upfront collaboration payments and future product commercialization.

Who are Triana Biomedicines's main competitors?

Direct peers on record are Arvinas, Kymera Therapeutics, Monte Rosa Therapeutics, C4 Therapeutics, Nurix Therapeutics, Fog Pharma, Amphista Therapeutics and Neomorph. Lycia Therapeutics is listed as an emerging player. Bristol Myers Squibb is listed as a broad incumbent.

Does Triana Biomedicines have an API?

No public API is recorded for Triana Biomedicines.

What industry is Triana Biomedicines in?

Triana Biomedicines's product category is Targeted Protein Degradation Therapeutics. Its primary akta.pro industry code is HLAAAIAH, Protein Interaction & Structural Biology Platforms (cryo-EM, X-ray, NMR, biophysics), with a secondary code of HLAAAIAI, Target Identification & Validation Platforms (omics-driven, chemoproteomics, genetic validation). Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
PR NewswireALK Inhibitors Market Set for Transformational Growth at a CAGR of 4% During the Forecast Period (2026-2036) Backed by Next-Generation Targeted Therapies| DelveInsightThe ALK inhibitors market is projected to grow at a 4% CAGR from 2026 to 2036, with the 7MM market valued at $3 billion in 2025. The US held the largest share at ~40%, and next-generation inhibitors like neladalkib and TRI-611 are expected to reshape the landscape.citybizTRIANA Biomedicines Adds Veteran Drug Developer Mohan Bala as COO Amid Molecular Glue PushTRIANA Biomedicines, a Lexington, Massachusetts-based biotech, appointed Mohan Bala as chief operating officer and expanded its scientific advisory board with oncology researchers Maria Koehler and David Tuveson, strengthening its leadership as it advances toward clinical development. Bala brings over 30 years of pharmaceutical experience including roles at Mersana Therapeutics and Constellation Pharmaceuticals, both of which were subsequently acquired, signaling TRIANA's shift toward later-stage operational and commercialization planning for its molecular glue degrader pipeline.BioSpaceTRIANA Biomedicines Announces the Appointment of Mohan Bala as Chief Operating Officer and Attracts Leading Experts to its Scientific Advisory BoardTRIANA Biomedicines appointed Mohan Bala as Chief Operating Officer and added Drs. Maria Koehler and David Tuveson to its Scientific Advisory Board. Bala brings over 30 years of industry experience, including roles at Mersana and Constellation Pharmaceuticals. The company aims to advance its molecular glue degrader pipeline, including TRI-611 for ALK+ NSCLC.Business Wire BlogTRIANA Biomedicines Announces the Appointment of Mohan Bala as Chief Operating Officer and Attracts Leading Experts to its Scientific Advisory BoardTRIANA Biomedicines appointed Dr. Mohan Bala as Chief Operating Officer and added Drs. Maria Koehler and David Tuveson to its Scientific Advisory Board to support the advancement of its molecular glue degrader pipeline. The leadership changes are intended to strengthen strategic, operational, and scientific capabilities for the company's drug development programs, including TRI-611. This move underscores TRIANA's focus on expanding its expertise in oncology therapies targeting difficult-to-drug disease targets.BioSpaceTRIANA Biomedicines Announces Oral Presentation of TRI-611 and Additional Poster Presentations at the American Association for Cancer Research Annual Meeting 2026TRIANA Biomedicines announced oral and poster presentations at the AACR Annual Meeting 2026 for its ALK molecular glue degrader TRI-611 and CCNE1 degrader. TRI-611 shows regression of ALK TKI-refractory tumors in preclinical models, and the company will present data on both assets.Business Wire BlogTRIANA Biomedicines Announces Oral Presentation of TRI-611 and Additional Poster Presentations at the American Association for Cancer Research Annual Meeting 2026TRIANA Biomedicines announced oral and poster presentations of its ALK molecular glue degrader TRI-611 and CCNE1 degrader at the AACR Annual Meeting 2026 in San Diego. The company highlighted preclinical data showing TRI-611 degrades TKI-resistant ALK fusion proteins and regresses ALK TKI-refractory tumors, with potential combinability with ALK TKIs.BioSpaceTRIANA Biomedicines’ TRI-611 Granted U.S. FDA Fast Track Designation for Treatment of ALK Positive Non-small Cell Lung CancerThe FDA granted Fast Track designation to TRIANA Biomedicines' TRI-611, an oral molecular glue degrader for ALK+ non-small cell lung cancer. The designation accelerates development and review, and the company's Phase 1/2 trial began in March 2026.PharmiWeb.comTRIANA Biomedicines’ TRI-611 Granted U.S. FDA Fast Track Designation for Treatment of ALK Positive Non-small Cell Lung CancerTRIANA Biomedicines announced that the U.S. FDA granted Fast Track designation for TRI-611, its investigational molecular glue degrader therapy for ALK-positive non-small cell lung cancer, designed for patients who have failed two or more ALK tyrosine kinase inhibitors. The first patient was treated with TRI-611 in a Phase 1/2 first-in-human clinical study in March 2026, which is evaluating safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity across dose escalation and efficacy cohorts. TRI-611 is an oral, brain-penetrant therapy that works by bringing ALK fusion proteins together with the E3 ligase cereblon to selectively eliminate the disease-causing protein through the body's innate protein-degradation machinery.BriefglanceTRIANA's 'Molecular Glue' Drug Enters Trials for Resistant Lung CancerTRIANA Biomedicines has announced the dosing of the first patient in a Phase 1/2 clinical trial for TRI-611, a novel molecular glue degrader therapy for ALK+ non-small cell lung cancer. The drug represents a new approach that works by tagging cancer-driving proteins for destruction rather than merely inhibiting them, addressing the critical challenge of acquired drug resistance in this patient population. TRI-611 is designed to be orally administered, brain-penetrant, and selective, specifically targeting the estimated 3-7% of NSCLC patients with the ALK+ subtype.BioSpaceTRIANA Biomedicines Announces First Patient Dosed in a Phase 1/2 Trial Evaluating TRI-611 for the Treatment of ALK Positive Non-small Cell Lung CancerTRIANA Biomedicines announced that the first patient has been dosed in a Phase 1/2 clinical trial evaluating TRI-611, a novel oral molecular glue degrader, in patients with ALK-positive non-small cell lung cancer. The global first-in-human trial will assess safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity across dose escalation and expansion phases. TRI-611 is designed to overcome resistance limitations of existing ALK tyrosine kinase inhibitors by harnessing the body's protein-degradation machinery to selectively eliminate ALK fusion proteins.