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Tris Pharma

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uuid00008b1

Namestring
Tris Pharma
Legal namestring
Tris Pharma, Inc.
Websiteurl
trispharma.com
Company typeenum
Private
Founded yearint
2000
Descriptiontext

Tris Pharma is a privately held, commercial-stage biopharmaceutical company founded in 2000 by Ketan Mehta and headquartered in Monmouth Junction, New Jersey. The company develops and commercializes specialty pharmaceuticals focused on central nervous system disorders, with a mature ADHD franchise (Dyanavel XR, Quillivant XR, QuilliChew ER, and Onyda XR — the only liquid non-stimulant ADHD medication) and a growing clinical pipeline spanning acute and chronic pain (cebranopadol, a first-in-class dual NOP/MOP receptor agonist with positive Phase 3 results), sleep disorders (TRN-257, a low-sodium, once-nightly oxybate with FDA Orphan Drug Designation), opioid use disorder, and other CNS indications.

The company's competitive foundation rests on two proprietary drug delivery platforms: LiquiXR, a particle-based technology that combines ionic chemistry with controlled-release science to produce extended-release oral suspensions, chewable tablets, and orally disintegrating tablets; and RaftWorks, an interpenetrating polymer network technology that creates an in-situ floating raft in the upper GI tract for sustained drug absorption. These platforms have generated 9+ FDA-approved NDAs and power more than a dozen approved or investigational therapies. Additional supporting technologies include Lipisol, maxsol, and eXsol for transforming medicines into patient-friendly oral dosage forms.

Tris generates revenue through three primary streams: branded pharmaceutical sales (ADHD products marketed directly to healthcare providers and distributed through US pharmacies and wholesalers), generic pharmaceutical sales (through wholly owned subsidiary Cranbury Pharmaceuticals, including the first generic version of Emflaza for Duchenne Muscular Dystrophy), and technology licensing/royalty income (out-licensing LiquiXR, RaftWorks, and finished products to regional partners in 33+ countries, including Kye Pharmaceuticals in Canada, Neuraxpharm across 40+ European countries, Pediatrix Therapeutics in China, and Perrigo for select US products). The company is expanding beyond small-molecule pharmaceuticals into digital health through an AI-enhanced ADHD diagnostic platform licensed from Braingaze.

Short descriptiontext

Tris Pharma is a private biopharmaceutical company developing and commercializing specialty CNS pharmaceuticals for ADHD, pain, addiction, and sleep disorders, anchored on proprietary LiquiXR and RaftWorks drug-delivery platforms and serving patients and healthcare providers across 33+ countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersMonmouth Junction, United States
HQ citystring
Monmouth Junction
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
specialty pharmaceuticals, CNS therapeutics, ADHD medications, drug delivery technology, extended-release formulations
Industry5 codes
1Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Connected Therapeutics & Smart Drug Delivery Monitoring
CodeHLACAFALPrimaryNo
4Specialty Pharmacy & Complex Therapy Management Platforms
CodeHLACAKAGPrimaryNo
5Clinical Development (Phase I–III Trial Design & Execution)
CodeHLAIALAEPrimaryNo
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing32541
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals - CNS Therapeutics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model4 records
1Branded Pharmaceutical Sales
TypeOne Time License
Description

Revenue from proprietary branded pharmaceutical products including ADHD medications (Dyanavel XR, Quillivant XR, QuilliChew ER, Onyda XR) marketed directly to healthcare providers and distributed through pharmacies.

trispharma.com
2Generic Pharmaceuticals
TypeOne Time License
Description

Revenue from generic pharmaceutical products through Cranbury Pharmaceuticals subsidiary, including first generic version of Emflaza for Duchenne Muscular Dystrophy and other generic medications.

trispharma.com
3Technology Licensing
TypeLicensing Royalties
Description

Revenue from licensing proprietary drug delivery technologies (LiquiXR®, RaftWorks™) to pharmaceutical partners worldwide for development and commercialization of their products.

trispharma.com
4International Partnerships
TypeLicensing Royalties
Description

Revenue from out-licensing approved products and pipeline candidates to international partners for development and commercialization in ex-US territories.

trispharma.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels6 records

Each record includes

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

Cost components6 values
Technology or R&D, Supply Chain, Operations, Personnel, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1LiquiXR
Description

Proprietary drug delivery technology platform enabling extended-release formulations in liquid, chewable tablet, film strip and orally disintegrating tablet dosage forms.

trispharma.com
+3 more records
Core offering1 text field

Tris Pharma develops, manufactures, and commercializes branded and generic specialty pharmaceuticals for central nervous system (CNS) disorders, with a commercial franchise in ADHD (Dyanavel XR, Quillivant XR, QuilliChew ER, Onyda XR) and a pipeline spanning pain (cebranopadol), sleep disorders (TRN-257), and other CNS indications. The company leverages proprietary drug delivery technology platforms (LiquiXR®, RaftWorks™, Lipisol™, maxsol™, eXsol™) to produce differentiated patient-friendly dosage forms including extended-release oral suspensions, chewable tablets, and orally disintegrating tablets. Tris also generates revenue through out-licensing its drug delivery technologies and products to international partners.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • Phase 3 ALLEVIATE-1 (abdominoplasty): LS mean difference 59.2 in pain score AUC vs placebo (p<0.001)
+6 more records
Product overview1 text field

Tris Pharma is a biopharmaceutical company with a diversified portfolio of ADHD medications and a pipeline spanning pain, addiction, and CNS disorders. The core ADHD portfolio includes four FDA-approved products: Dyanavel XR (amphetamine, oral suspension and tablets), Quillivant XR (methylphenidate oral suspension), QuilliChew ER (methylphenidate chewable tablets), and ONYDA XR (clonidine oral suspension - the only liquid non-stimulant ADHD option). The pipeline includes TRN-257 (low-sodium oxybate for narcolepsy/idiopathic hypersomnia, NDA accepted by FDA), cebranopadol (first-in-class dual-NMR agonist for pain, Phase 3 completed for acute pain), TRN-213 (for spasticity, Phase 2), TRN-218 (pediatric ADHD, Phase 2), and TRN-261 (peptide analgesic). The company also operates a digital health business developing an AI-enhanced ADHD diagnostic platform. Technology platforms include LiquiXR (particle-based extended-release technology powering over a dozen therapies) and RaftWorks (controlled absorption technology). The generics business is managed through subsidiary Cranbury Pharmaceuticals.

Product and service10 records
1DYANAVEL XR (amphetamine)
CategoryBranded ADHD Pharmaceutical
Description

Once-daily extended-release amphetamine ADHD medication available as oral suspension and chewable/swallowable tablets for patients 6 years and older. Uses LiquiXR® technology for extended-release delivery and can be chewed or swallowed whole.

2Quillivant XR (methylphenidate)
CategoryBranded ADHD Pharmaceutical
Description

Extended-release methylphenidate oral suspension for ADHD treatment, using LiquiXR® technology for once-daily dosing. Marketed by NextWave Pharmaceuticals, a wholly owned subsidiary of Tris Pharma.

3QuilliChew ER (methylphenidate)
CategoryBranded ADHD Pharmaceutical
Description

First FDA-approved extended-release chewable methylphenidate tablet for ADHD, using LiquiXR® technology for flexible dosing. Marketed by NextWave Pharmaceuticals, a wholly owned subsidiary of Tris Pharma.

4ONYDA XR (clonidine hydrochloride)
CategoryBranded ADHD Pharmaceutical
Description

First and only FDA-approved liquid non-stimulant ADHD medication (extended-release oral suspension). Approved as monotherapy or adjunctive therapy to stimulant medications for patients 6 years and older. Uses LiquiXR® technology.

5Cebranopadol
CategoryPipeline CNS Pharmaceutical - Pain
Description

First-in-class dual NOP/MOP receptor agonist (dual-NMR) for moderate-to-severe acute pain, chronic pain, neuropathic pain, and opioid use disorder. Phase 3 completed for acute pain (ALLEVIATE-1 and ALLEVIATE-2 trials met primary endpoints). Fast Track Designation granted for chronic low back pain. Studied in over 2,200 patients across 33 clinical trials.

6TRN-257 (Oxybate Extended-Release)
CategoryPipeline CNS Pharmaceutical - Sleep Disorders
Description

Investigational once-nightly, low-sodium oxybate product for treating narcolepsy and idiopathic hypersomnia. Uses RaftWorks™ and LiquiXR® platforms. Contains 80mg sodium per 9g dose (lowest among oxybate products in development). FDA NDA accepted December 2025; Orphan Drug Designation granted June 2026.

7TRN-261
CategoryPipeline CNS Pharmaceutical - Pain
Description

First-in-class peptide molecule analgesic in development for multiple acute and chronic pain indications. Extensively studied clinically in non-pain indications with strong potential for effective pain relief.

8TRN-213
CategoryPipeline CNS Pharmaceutical - Other CNS Disorders
Description

Optimized formulation for spasticity treatment associated with multiple sclerosis and other diseases like cerebral palsy. Designed as extended-release treatment option for more consistent daily efficacy, higher adherence, and reduced side effects. Phase 2 stage.

9TRN-218
CategoryPipeline ADHD Pharmaceutical
Description

Once-daily oral suspension extended-release ADHD treatment under investigation for pediatric patients with ADHD. Designed with profile expected to be favorable for autism spectrum disorder (ASD) patients. Phase 2 stage.

10Cranbury Pharmaceuticals Generics Portfolio
CategoryGeneric Pharmaceuticals
Description

Subsidiary handling Tris Pharma's generics portfolio and pipeline, including the first generic version of Emflaza (deflazacort) oral suspension for Duchenne Muscular Dystrophy. Operates as Cranbury Pharmaceuticals, debuted June 2024.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierMajorTypeChannel Partner/ Reseller/ DistributorAnnounced on2023-10-30
Description

Partnership to enhance accessibility, affordability and adherence for Dyanavel XR tablets via digital pharmacy services, providing patients with convenient prescription management and delivery options.

Strategic tierMajorTypeImplementation/ SI/ Consulting PartnerAnnounced on2022-12-07
Description

CenExel conducted ALLEVIATE-2 Phase 3 clinical trial for cebranopadol at multiple U.S. research sites, with Dr. Todd Bertoch serving as Chief Medical Officer and Principal Investigator.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2022-12-01
Description

Expansion of partnership to commercialize Tris' FDA-approved ADHD medicines and investigational ADHD therapy in China. Original partnership established December 2020 and expanded in December 2022.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-04-29
Description

Acquisition of Park Therapeutics including first-in-class, Phase III-ready new chemical entity for pain, expanding Tris' pain pipeline. This acquisition brought cebranopadol into Tris' development portfolio.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-12-08
Description

Partnership to commercialize Tris' Quillivant XR and Quillichew ER in 40+ European countries. Neuraxpharm holds rights to develop and commercialize approved ADHD products across major European markets.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-07-09
Description

Exclusive license agreement to commercialize Tris ADHD products in Canada. Kye Pharmaceuticals serves as Tris Pharma's first ex-U.S. partner for approved ADHD portfolio, bringing Dyanavel XR tablets to Canadian patients in 2026.

Strategic tierMajorTypeChannel Partner/ Reseller/ Distributor
Description

Long-standing commercial partnership since 2012 for various pharmaceutical products.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Licensed rights to develop and commercialize Braingaze's first-in-class AI-enhanced digital ADHD diagnostic platform in the United States and Canada, expanding Tris' digital health offerings.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Direct TRN-257 competitor through Xywav (oxybate) franchise for narcolepsy and idiopathic hypersomnia. Comparable CNS specialty pharma with strong orphan drug positioning and ADHD-adjacent CNS portfolio.

TypeDirect peer
Description

Specialty CNS pharma with overlapping ADHD portfolio (Qelbree, Adzenys) and adjacent CNS pipeline. Closely comparable business model of branded specialty pharma with proprietary delivery technologies and CNS focus.

TypeDirect peer
Description

Specialty pharma with pain franchise (Belbuca, buprenorphine) and proprietary drug delivery platforms. Comparable model of branded specialty pharma using differentiated formulation to compete in CNS/pain markets.

TypeDirect peer
Description

Direct TRN-257 competitor with FT218 (Lumryz), an extended-release once-nightly sodium oxybate for narcolepsy. Highly comparable in patient-friendly reformulation strategy targeting same oxybate market.

TypeBroad incumbent
Description

Large established CNS specialty pharma (Onfi, Sabril, Rexulti) with portfolio overlap in CNS disorders including ADHD-adjacent and sleep. Broader portfolio than Tris but similar patient-focused CNS specialty approach.

TypeDirect peer
Description

Generic pharmaceutical company directly comparable to Tris's Cranbury Pharmaceuticals subsidiary. Similar generics portfolio strategy and CNS/general medicine focus.

TypeBroad incumbent
Description

Specialty pharma with overlapping CNS portfolio (ADHD, pain) and generic specialty pharmaceuticals business. Notable as multiple Tris executives (Manesh Naidu, Jim Potenziano) previously worked there.

TypeEmerging player
Description

Specialty CNS pharma developing prodrug ADHD stimulants (Azstarys) with proprietary delivery technology. Direct competitive overlap in ADHD with smaller commercial footprint than Tris.

TypeDirect peer
Description

CNS specialty pharma with pain focus (Xtampza, Belbuca) and ADHD presence via Ironshore acquisition ( Jornay PM, Adhansia XR). Comparable commercial-stage specialty CNS business model and patient-friendly formulation strategy.

TypeDirect peer
Description

Acquired Neos Therapeutics' ADHD portfolio (Adzenys, Cotempla) — directly competes with Tris's Quillivant XR and Dyanavel XR in the branded stimulant ADHD market. Similar mid-sized specialty CNS profile.

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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

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

Segment4 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

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

Subsidiaries2 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance6 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

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

Investors2 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 →

Tris Pharma

Specialty Pharmaceuticals - CNS Therapeuticstrispharma.com

Tris Pharma is a private biopharmaceutical company developing and commercializing specialty CNS pharmaceuticals for ADHD, pain, addiction, and sleep disorders, anchored on proprietary LiquiXR and RaftWorks drug-delivery platforms and serving patients and healthcare providers across 33+ countries.

What Tris Pharma does

Tris Pharma is a privately held, commercial-stage biopharmaceutical company founded in 2000 by Ketan Mehta and headquartered in Monmouth Junction, New Jersey. The company develops and commercializes specialty pharmaceuticals focused on central nervous system disorders, with a mature ADHD franchise (Dyanavel XR, Quillivant XR, QuilliChew ER, and Onyda XR — the only liquid non-stimulant ADHD medication) and a growing clinical pipeline spanning acute and chronic pain (cebranopadol, a first-in-class dual NOP/MOP receptor agonist with positive Phase 3 results), sleep disorders (TRN-257, a low-sodium, once-nightly oxybate with FDA Orphan Drug Designation), opioid use disorder, and other CNS indications.

The company's competitive foundation rests on two proprietary drug delivery platforms: LiquiXR, a particle-based technology that combines ionic chemistry with controlled-release science to produce extended-release oral suspensions, chewable tablets, and orally disintegrating tablets; and RaftWorks, an interpenetrating polymer network technology that creates an in-situ floating raft in the upper GI tract for sustained drug absorption. These platforms have generated 9+ FDA-approved NDAs and power more than a dozen approved or investigational therapies. Additional supporting technologies include Lipisol, maxsol, and eXsol for transforming medicines into patient-friendly oral dosage forms.

Tris generates revenue through three primary streams: branded pharmaceutical sales (ADHD products marketed directly to healthcare providers and distributed through US pharmacies and wholesalers), generic pharmaceutical sales (through wholly owned subsidiary Cranbury Pharmaceuticals, including the first generic version of Emflaza for Duchenne Muscular Dystrophy), and technology licensing/royalty income (out-licensing LiquiXR, RaftWorks, and finished products to regional partners in 33+ countries, including Kye Pharmaceuticals in Canada, Neuraxpharm across 40+ European countries, Pediatrix Therapeutics in China, and Perrigo for select US products). The company is expanding beyond small-molecule pharmaceuticals into digital health through an AI-enhanced ADHD diagnostic platform licensed from Braingaze.

Tris Pharma firmographics

Firmographics
Name
Tris Pharma
Legal name
Tris Pharma, Inc.
Website
https://trispharma.com
Company type
Private
Founded year
2000
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Tris Pharma is a private biopharmaceutical company developing and commercializing specialty CNS pharmaceuticals for ADHD, pain, addiction, and sleep disorders, anchored on proprietary LiquiXR and RaftWorks drug-delivery platforms and serving patients and healthcare providers across 33+ countries.
Ownership category
akta.pro rank

Tris Pharma industry classification

Industry
Product category
Specialty Pharmaceuticals - CNS Therapeutics
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (32541), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Connected Therapeutics & Smart Drug Delivery Monitoring (HLACAFAL), Specialty Pharmacy & Complex Therapy Management Platforms (HLACAKAG), Clinical Development (Phase I–III Trial Design & Execution) (HLAIALAE)

Keywords

  • Specialty pharmaceuticals
  • CNS therapeutics
  • ADHD medications
  • Drug delivery technology
  • Extended-release formulations

Where Tris Pharma is headquartered

Location

Headquarters

HQ city
Monmouth Junction
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Tris Pharma business model

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

Revenue model

  1. Branded Pharmaceutical Sales: Revenue from proprietary branded pharmaceutical products including ADHD medications (Dyanavel XR, Quillivant XR, QuilliChew ER, Onyda XR) marketed directly to healthcare providers and distributed through pharmacies.
  2. Generic Pharmaceuticals: Revenue from generic pharmaceutical products through Cranbury Pharmaceuticals subsidiary, including first generic version of Emflaza for Duchenne Muscular Dystrophy and other generic medications.
  3. Technology Licensing: Revenue from licensing proprietary drug delivery technologies (LiquiXR®, RaftWorks™) to pharmaceutical partners worldwide for development and commercialization of their products.
  4. International Partnerships: Revenue from out-licensing approved products and pipeline candidates to international partners for development and commercialization in ex-US territories.

Go-to-market motion1 record

Distribution channels6 records

Marketing channels6 records

Tris Pharma product offering

Product offering

Core offering

Tris Pharma develops, manufactures, and commercializes branded and generic specialty pharmaceuticals for central nervous system (CNS) disorders, with a commercial franchise in ADHD (Dyanavel XR, Quillivant XR, QuilliChew ER, Onyda XR) and a pipeline spanning pain (cebranopadol), sleep disorders (TRN-257), and other CNS indications. The company leverages proprietary drug delivery technology platforms (LiquiXR®, RaftWorks™, Lipisol™, maxsol™, eXsol™) to produce differentiated patient-friendly dosage forms including extended-release oral suspensions, chewable tablets, and orally disintegrating tablets. Tris also generates revenue through out-licensing its drug delivery technologies and products to international partners.

Product overview

Tris Pharma is a biopharmaceutical company with a diversified portfolio of ADHD medications and a pipeline spanning pain, addiction, and CNS disorders. The core ADHD portfolio includes four FDA-approved products: Dyanavel XR (amphetamine, oral suspension and tablets), Quillivant XR (methylphenidate oral suspension), QuilliChew ER (methylphenidate chewable tablets), and ONYDA XR (clonidine oral suspension - the only liquid non-stimulant ADHD option). The pipeline includes TRN-257 (low-sodium oxybate for narcolepsy/idiopathic hypersomnia, NDA accepted by FDA), cebranopadol (first-in-class dual-NMR agonist for pain, Phase 3 completed for acute pain), TRN-213 (for spasticity, Phase 2), TRN-218 (pediatric ADHD, Phase 2), and TRN-261 (peptide analgesic). The company also operates a digital health business developing an AI-enhanced ADHD diagnostic platform. Technology platforms include LiquiXR (particle-based extended-release technology powering over a dozen therapies) and RaftWorks (controlled absorption technology). The generics business is managed through subsidiary Cranbury Pharmaceuticals.

Differentiator

Problem solved

Functional benefit

Brands

  • LiquiXR: Proprietary drug delivery technology platform enabling extended-release formulations in liquid, chewable tablet, film strip and orally disintegrating tablet dosage forms.
  • RaftWorks
  • Cranbury Pharmaceuticals
  • NextWave Pharmaceuticals

Products and services

  • DYANAVEL XR (amphetamine) Once-daily extended-release amphetamine ADHD medication available as oral suspension and chewable/swallowable tablets for patients 6 years and older. Uses LiquiXR® technology for extended-release delivery and can be chewed or swallowed whole.
  • Quillivant XR (methylphenidate) Extended-release methylphenidate oral suspension for ADHD treatment, using LiquiXR® technology for once-daily dosing. Marketed by NextWave Pharmaceuticals, a wholly owned subsidiary of Tris Pharma.
  • QuilliChew ER (methylphenidate) First FDA-approved extended-release chewable methylphenidate tablet for ADHD, using LiquiXR® technology for flexible dosing. Marketed by NextWave Pharmaceuticals, a wholly owned subsidiary of Tris Pharma.
  • ONYDA XR (clonidine hydrochloride) First and only FDA-approved liquid non-stimulant ADHD medication (extended-release oral suspension). Approved as monotherapy or adjunctive therapy to stimulant medications for patients 6 years and older. Uses LiquiXR® technology.
  • Cebranopadol First-in-class dual NOP/MOP receptor agonist (dual-NMR) for moderate-to-severe acute pain, chronic pain, neuropathic pain, and opioid use disorder. Phase 3 completed for acute pain (ALLEVIATE-1 and ALLEVIATE-2 trials met primary endpoints). Fast Track Designation granted for chronic low back pain. Studied in over 2,200 patients across 33 clinical trials.
  • TRN-257 (Oxybate Extended-Release) Investigational once-nightly, low-sodium oxybate product for treating narcolepsy and idiopathic hypersomnia. Uses RaftWorks™ and LiquiXR® platforms. Contains 80mg sodium per 9g dose (lowest among oxybate products in development). FDA NDA accepted December 2025; Orphan Drug Designation granted June 2026.
  • TRN-261 First-in-class peptide molecule analgesic in development for multiple acute and chronic pain indications. Extensively studied clinically in non-pain indications with strong potential for effective pain relief.
  • TRN-213 Optimized formulation for spasticity treatment associated with multiple sclerosis and other diseases like cerebral palsy. Designed as extended-release treatment option for more consistent daily efficacy, higher adherence, and reduced side effects. Phase 2 stage.
  • TRN-218 Once-daily oral suspension extended-release ADHD treatment under investigation for pediatric patients with ADHD. Designed with profile expected to be favorable for autism spectrum disorder (ASD) patients. Phase 2 stage.
  • Cranbury Pharmaceuticals Generics Portfolio Subsidiary handling Tris Pharma's generics portfolio and pipeline, including the first generic version of Emflaza (deflazacort) oral suspension for Duchenne Muscular Dystrophy. Operates as Cranbury Pharmaceuticals, debuted June 2024.

Quantifiable outcome

  • Phase 3 ALLEVIATE-1 (abdominoplasty): LS mean difference 59.2 in pain score AUC vs placebo (p<0.001)
  • +6 more outcomes

Companies that use Tris Pharma

Customer profile

Named customers5 records

Segments4 records

Ideal customer profiles2 records

Tris Pharma technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Tris Pharma partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered major and core.

  • Perigon Pharmacy 360majorChannel Partner/ Reseller/ Distributor · 30 October 2023Partnership to enhance accessibility, affordability and adherence for Dyanavel XR tablets via digital pharmacy services, providing patients with convenient prescription management and delivery options.
  • CenExel Clinical ResearchmajorImplementation/ SI/ Consulting Partner · 7 December 2022CenExel conducted ALLEVIATE-2 Phase 3 clinical trial for cebranopadol at multiple U.S. research sites, with Dr. Todd Bertoch serving as Chief Medical Officer and Principal Investigator.
  • Pediatrix TherapeuticscoreChannel Partner/ Reseller/ Distributor · 1 December 2022Expansion of partnership to commercialize Tris' FDA-approved ADHD medicines and investigational ADHD therapy in China. Original partnership established December 2020 and expanded in December 2022.
  • Park TherapeuticscoreStrategic or Co-development Partner · 29 April 2021Acquisition of Park Therapeutics including first-in-class, Phase III-ready new chemical entity for pain, expanding Tris' pain pipeline. This acquisition brought cebranopadol into Tris' development portfolio.
  • Neuraxpharm GroupcoreChannel Partner/ Reseller/ Distributor · 8 December 2020Partnership to commercialize Tris' Quillivant XR and Quillichew ER in 40+ European countries. Neuraxpharm holds rights to develop and commercialize approved ADHD products across major European markets.
  • Kye PharmaceuticalscoreChannel Partner/ Reseller/ Distributor · 9 July 2020Exclusive license agreement to commercialize Tris ADHD products in Canada. Kye Pharmaceuticals serves as Tris Pharma's first ex-U.S. partner for approved ADHD portfolio, bringing Dyanavel XR tablets to Canadian patients in 2026.
  • Perrigo CompanymajorChannel Partner/ Reseller/ DistributorLong-standing commercial partnership since 2012 for various pharmaceutical products.
  • BraingazecoreStrategic or Co-development PartnerLicensed rights to develop and commercialize Braingaze's first-in-class AI-enhanced digital ADHD diagnostic platform in the United States and Canada, expanding Tris' digital health offerings.

Scale indicators11 records

Recent moves7 records

Expansion highlights6 records

Tris Pharma competitors and assessment

Company assessment

Direct peers

  • Jazz Pharmaceuticals: Direct TRN-257 competitor through Xywav (oxybate) franchise for narcolepsy and idiopathic hypersomnia. Comparable CNS specialty pharma with strong orphan drug positioning and ADHD-adjacent CNS portfolio.
  • Supernus Pharmaceuticals: Specialty CNS pharma with overlapping ADHD portfolio (Qelbree, Adzenys) and adjacent CNS pipeline. Closely comparable business model of branded specialty pharma with proprietary delivery technologies and CNS focus.
  • BioDelivery Sciences International: Specialty pharma with pain franchise (Belbuca, buprenorphine) and proprietary drug delivery platforms. Comparable model of branded specialty pharma using differentiated formulation to compete in CNS/pain markets.
  • Avadel Pharmaceuticals: Direct TRN-257 competitor with FT218 (Lumryz), an extended-release once-nightly sodium oxybate for narcolepsy. Highly comparable in patient-friendly reformulation strategy targeting same oxybate market.
  • Camber Pharmaceuticals: Generic pharmaceutical company directly comparable to Tris's Cranbury Pharmaceuticals subsidiary. Similar generics portfolio strategy and CNS/general medicine focus.
  • Collegium Pharmaceutical: CNS specialty pharma with pain focus (Xtampza, Belbuca) and ADHD presence via Ironshore acquisition ( Jornay PM, Adhansia XR). Comparable commercial-stage specialty CNS business model and patient-friendly formulation strategy.
  • Aytu BioPharma: Acquired Neos Therapeutics' ADHD portfolio (Adzenys, Cotempla) — directly competes with Tris's Quillivant XR and Dyanavel XR in the branded stimulant ADHD market. Similar mid-sized specialty CNS profile.

Broad incumbents

  • Lundbeck: Large established CNS specialty pharma (Onfi, Sabril, Rexulti) with portfolio overlap in CNS disorders including ADHD-adjacent and sleep. Broader portfolio than Tris but similar patient-focused CNS specialty approach.
  • Mallinckrodt Pharmaceuticals: Specialty pharma with overlapping CNS portfolio (ADHD, pain) and generic specialty pharmaceuticals business. Notable as multiple Tris executives (Manesh Naidu, Jim Potenziano) previously worked there.

Emerging players

  • KemPharm: Specialty CNS pharma developing prodrug ADHD stimulants (Azstarys) with proprietary delivery technology. Direct competitive overlap in ADHD with smaller commercial footprint than Tris.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key highlights7 records

Customer concentration

Tris Pharma social profiles

Digital presence

Tris Pharma compliance and trust

Trust signal

Compliance6 records

Tris Pharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Tris Pharma leadership team

Management profile

Number of profiles

Profiles12 records

Tris Pharma subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

Tris Pharma funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors2 records

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Tris Pharma M&A and investment

M&A and investment

M&A1 record

Investments

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Frequently asked questions about Tris Pharma

What does Tris Pharma do?

Tris Pharma develops, manufactures, and commercializes branded and generic specialty pharmaceuticals for central nervous system (CNS) disorders, with a commercial franchise in ADHD (Dyanavel XR, Quillivant XR, QuilliChew ER, Onyda XR) and a pipeline spanning pain (cebranopadol), sleep disorders (TRN-257), and other CNS indications. The company leverages proprietary drug delivery technology platforms (LiquiXR®, RaftWorks™, Lipisol™, maxsol™, eXsol™) to produce differentiated patient-friendly dosage forms including extended-release oral suspensions, chewable tablets, and orally disintegrating tablets. Tris also generates revenue through out-licensing its drug delivery technologies and products to international partners.

Is Tris Pharma a public or private company?

Tris Pharma is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Tris Pharma founded?

Tris Pharma was founded in 2000. It employs 501 to 1,000 people.

Where is Tris Pharma based?

Tris Pharma is headquartered in Monmouth Junction, United States, in the North America region.

How does Tris Pharma make money?

Four revenue lines are on record. Branded Pharmaceutical Sales are the primary driver. The others are generic Pharmaceuticals, technology Licensing and international Partnerships.

Who are Tris Pharma's main competitors?

Direct peers on record are Jazz Pharmaceuticals, Supernus Pharmaceuticals, BioDelivery Sciences International, Avadel Pharmaceuticals, Camber Pharmaceuticals, Collegium Pharmaceutical and Aytu BioPharma. Broad incumbents are Lundbeck and Mallinckrodt Pharmaceuticals. KemPharm is listed as an emerging player.

Does Tris Pharma have an API?

No public API is recorded for Tris Pharma.

What industry is Tris Pharma in?

Tris Pharma's product category is Specialty Pharmaceuticals - CNS Therapeutics. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
YahooTris Pharma To Pay Texas $7.5 Million Over Alleged Misleading ADHD Drug ClaimsTexas Attorney General Ken Paxton reached a $7.5 million settlement with Tris Pharmaceuticals over allegations of misrepresenting the effectiveness of Dyanavel XR, an ADHD medication for children. The company will pay the state to resolve claims that it overstated the drug's speed and benefits during sales calls.EIN PresswireBrown, LLC Helps Secure $7.5 Million Texas Whistleblower Settlement with Tris Pharma Over ADHD Drug MarketingBrown, LLC announced a $7.5 million settlement with Tris Pharma and Ketan Mehta over false ADHD drug marketing claims under Texas law. The settlement resolves the action in full, and together with a prior $41.5 million Pfizer settlement, the two Texas matters total $49 million. Texas will allocate the federal share of the recovery to the United States.BioSpaceTris Pharma Introduces New 30-Count Bottle Size for QuilliChew ER® (methylphenidate HCl) Extended-Release Chewable Tablets for Attention Deficit Hyperactivity Disorder (ADHD)Tris Pharma introduced a new 30-count bottle of QuilliChew ER chewable tablets for ADHD, available in 20, 30, and 40 mg strengths. The size aligns with a 30-day supply and is available through major wholesalers, with the 100-count bottle phased out. The manufacturer's price per tablet remains unchanged.BioSpaceTris Pharma Expands Support for People Living with ADHD Through New Partnerships with Calm Health and ADHD CentralTris Pharma announced partnerships with Calm Health and ADHD Central to provide digital wellness and organization tools for ADHD patients. Eligible patients starting DYANAVEL XR will receive three months of complimentary Calm Health access. The initiative aims to support mental well-being and daily organization beyond medication.The Pharma LetterAdneuris to receive $35M from cebranopadol dealAdneuris Therapeutics, a subsidiary of Tris Pharma, announced an exclusive licensing agreement with Japan’s Maruishi Pharmaceutical to develop and commercialize cebranopadol for pain treatment in Japan and South Korea.Endpoints NewsTris Pharma’s CRL for narcolepsy drug; Agenus abandons Phase 3 CRC trialThe FDA issued a Complete Response Letter (CRL) rejecting Tris Pharma's application for its narcolepsy drug. Additionally, Agenus announced the abandonment of its Phase 3 clinical trial for colorectal cancer (CRC).GlobeNewswireTris Pharma Launches Adneuris Therapeutics to Advance a New Era in Pain MedicineAdneuris Therapeutics, a wholly owned subsidiary of Tris Pharma, launched to develop and commercialize cebranopadol, its lead investigational first-in-class dual NOP/MOP receptor agonist for treating moderate-to-severe acute pain. The drug has completed Phase 3 clinical trials enrolling more than 2,400 participants across two pivotal studies, demonstrating significant pain reduction compared to placebo over 48 hours and reduced use of opioid rescue medication. Tris Pharma received a five-year grant of up to $16.6 million from the National Institute on Drug Abuse (NIDA) to study cebranopadol's potential to treat opioid use disorder and substance use disorders.YicaiglobalChina’s Conba Secures Rights to Tris Pharma's Experimental Painkiller in ChinaChinese drugmaker Conba Pharmaceutical has signed an exclusive licensing deal with Adneuris Therapeutics, a unit of Tris Pharma, to develop, register, and commercialize the experimental analgesic Cebranopadol across mainland China, Hong Kong, Taiwan, and Macao. Conba will pay up to USD111.5 million, comprising a USD17.5 million upfront fee and milestone payments of up to USD94 million tied to regulatory approvals and annual sales targets. The drug, which targets opioid receptors for postoperative acute pain treatment, has completed Phase III trials and is expected to seek FDA approval later this year.GlobeNewswireTris Pharma Announces FDA Grant of Orphan Drug Designation for TRN-257 (Oxybate for Extended-Release Oral Suspension) a Once-Nightly, Low-Sodium Oxybate Product for Idiopathic HypersomniaTris Pharma announced that the U.S. FDA granted Orphan Drug Designation to TRN-257, an extended-release oxybate product candidate for treating idiopathic hypersomnia, based on the hypothesis that it may be clinically superior to existing oxybate products. The product is designed for once-nightly dosing to eliminate the need for patients to wake in the middle of the night, while also offering the lowest sodium content (80mg per 9g dose) among oxybate products in development. The designation confers eligibility for a seven-year period of market exclusivity in the U.S. upon approval and reflects the FDA's recognition of TRN-257's potential major contribution to patient care for a rare, chronic sleep disorder affecting fewer than 200,000 Americans.GlobeNewswireTris Pharma Introduces a New 60 mL Bottle Size for DYANAVEL® XR (amphetamine) Extended-Release Oral Suspension CIITris Pharma announced the availability of a new 60 mL bottle size for DYANAVEL XR (amphetamine) extended-release oral suspension, a once-daily ADHD treatment for patients 6 years and older. The smaller bottle size is designed to improve pharmacy stocking and dispensing convenience, providing 30 days of the starting dose of 5 mg/day, while the larger 464 mL bottle will be phased out. The manufacturer states no changes were made to the formulation or cost per mL of the medication.