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Retrophin

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Namestring
Retrophin
Legal namestring
Travere Therapeutics, Inc.
Websiteurl
Retrophin.com
Company typeenum
Public
Founded yearint
2012
Descriptiontext

Retrophin (now operating as Travere Therapeutics, Inc.) is a publicly traded biopharmaceutical company headquartered in San Diego, California, that focuses on developing and commercializing therapies for people living with rare diseases. Founded in 2012 and rebranded from its original Retrophin identity to Travere Therapeutics in 2022, the company is listed on NASDAQ (evidenced by Nasdaq Listing Rule 5635(c)(4) disclosures) and operates across four therapeutic areas: IgA Nephropathy (IgAN), Focal Segmental Glomerulosclerosis (FSGS), Classical Homocystinuria (HCU), and Cystinuria. The company has a stated headcount of 101-250 employees and structures its go-to-market around direct physician and patient outreach, patient advocacy partnerships, and specialty care channels in rare kidney disease communities.

The commercial portfolio centers on FILSPARI (sparsentan), an endothelin angiotensin receptor antagonist that has received full U.S. FDA approval for both FSGS — where it is the first and only approved medicine — and IgA Nephropathy. Travere also markets Thiola and Thiola EC for cystinuria (registered trademarks of Mission Pharmacal Company, held under license or distribution arrangement). The development pipeline is anchored by Pegtibatinase, an investigational enzyme replacement therapy for Classical Homocystinuria, expanding the proprietary science base into rare metabolic disease. Filspari, Total Care Hub, and Travere TotalCare are registered trademarks of Travere Therapeutics.

Revenue is generated through prescription pharmaceutical product sales of FDA-approved therapies (FILSPARI; Thiola / Thiola EC) distributed within the United States via specialty pharmacy channels to healthcare providers and patients. Patient access is supported by branded programs — Total Care Hub and Travere TotalCare — providing adherence and care-coordination services. The company engages the market through a multi-channel model: organic social (Facebook, Instagram, LinkedIn, X, YouTube), content marketing through the Rare Life patient-story program, medical affairs engagement including presentations at major scientific congresses such as the European Renal Association, and earned media / investor relations. Specific drug pricing is not publicly disclosed and is accessed via healthcare providers and specialty pharmacies using standard insurance coverage mechanics.

Short descriptiontext

Travere Therapeutics (formerly Retrophin) is a publicly traded, San Diego-based biopharmaceutical company developing and commercializing FDA-approved therapies for rare kidney and metabolic diseases including FSGS, IgA Nephropathy, and cystinuria.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
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
rare disease therapeutics, kidney disease treatments, orphan drug development, specialty pharmaceuticals, enzyme replacement therapy
Industry4 codes
1Rare Renal & Nephrology Disorder Therapies
CodeHLAIAIAIPrimaryYes
2Nephrology & Urology Specialty Pharmaceuticals
CodeHLAIACAHPrimaryNo
3Nephrology & Urology Pharmaceuticals
CodeHLAIAAAMPrimaryNo
4Genetic & Rare Kidney Disease Clinics
CodeHLAKAHAOPrimaryNo
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Rare Disease Specialty Pharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Sales
TypeOne Time License
Description

Revenue generated from the sale of FDA-approved prescription medications including FILSPARI (sparsentan) for FSGS and IgAN, and Thiola/Thiola EC for cystinuria. The company develops and commercializes therapies for rare kidney diseases and metabolic disorders.

travere.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Marketing or Sales, Operations, Supply Chain
GTM typeB2B and B2C
B2B and B2C
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1Total Care Hub
Description

Registered trademark; patient support and care program

travere.com
+3 more records
Core offering1 text field

Retrophin (operating as Travere Therapeutics) develops and commercializes FDA-approved prescription therapies for rare kidney diseases and rare metabolic disorders. Core commercial products include FILSPARI (sparsentan) for Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN), and Thiola/Thiola EC for cystinuria. The company's pipeline includes Pegtibatinase, an investigational enzyme replacement therapy for Classical Homocystinuria (HCU).

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Travere Therapeutics (formerly Retrophin) is a patient-centered biopharmaceutical company focused on developing therapies for rare kidney diseases. The company's product portfolio includes FILSPARI (sparsentan), an FDA-approved treatment for Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN), and Thiola/Thiola EC for cystinuria. The pipeline includes Pegtibatinase for Classical Homocystinuria (HCU). The company operates across four main therapeutic areas: IgA Nephropathy, FSGS, Classical Homocystinuria, and Cystinuria.

Product and service4 records
1FILSPARI (sparsentan)
CategoryRare Kidney Disease Therapeutics
Description

FILSPARI (sparsentan) is an FDA-approved endothelin angiotensin receptor antagonist indicated for the treatment of Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN). It is the first and only approved medicine for FSGS, targeting patients with rare kidney diseases who have limited therapeutic options.

2Thiola
CategoryRare Metabolic Disorder Therapeutics
Description

Thiola is a registered trademark prescription medication for the treatment of cystinuria, a rare metabolic disorder. It is licensed or acquired from Mission Pharmacal Company.

3Thiola EC
CategoryRare Metabolic Disorder Therapeutics
Description

Thiola EC is an enteric-coated formulation of the cystinuria treatment medication Thiola, providing an alternative dosing form for patients with cystinuria. Thiola EC is a registered trademark of Mission Pharmacal Company.

4Pegtibatinase
CategoryInvestigational Enzyme Replacement Therapy
Description

Pegtibatinase is an investigational enzyme replacement therapy in clinical development for the treatment of Classical Homocystinuria (HCU), a rare inherited metabolic disorder.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-06-04
Description

Travere Therapeutics presented long-term open-label extension data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress, showcasing clinical trial results for their therapeutic candidates.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Calliditas developed Tarpeyo, an FDA-approved targeted-release budesonide for IgA Nephropathy, directly competing with Travere's FILSPARI in the same rare kidney indication and overlapping specialty nephrology customer base.

TypeDirect peer
Description

Pre-acquisition by Novartis, Chinook was a clinical-stage rare kidney disease company developing therapies for IgAN and other rare nephropathies, making it a direct comparator in rare kidney pipeline strategy and indication focus.

TypeDirect peer
Description

Vera is developing atacicept for IgA Nephropathy, positioning it as a direct competitor to FILSPARI in IgAN with a similar specialty nephrology commercial target and patient advocacy model.

TypeDirect peer
Description

Reata developed and commercialized bardoxolone methyl for rare forms of CKD, making it a comparable rare kidney disease biopharma with overlapping nephrology prescribers and similar regulatory pathway focus.

TypeBroad incumbent
Description

Otsuka markets tolvaptan for ADPKD, a rare kidney disease, and operates a broad rare disease and specialty pharma portfolio that overlaps with Travere's nephrology focus and specialty pharmacy distribution model.

TypeBroad incumbent
Description

Alexion is a global rare disease leader with complement-mediated kidney therapies (e.g., Soliris/Ultomiris in aHUS) and overlapping rare disease patient advocacy and specialty distribution infrastructure.

TypeBroad incumbent
Description

BioMarin is an established rare disease biopharma with a multi-indication orphan drug portfolio and a similar specialty distribution and patient access model relevant to Travere's commercial approach.

TypeBroad incumbent
Description

Vertex is expanding from its rare disease CF franchise into additional rare and specialty indications (including nephrology-adjacent assets via Alpine acquisition), making it a comparable scaling rare disease biopharma with similar capital markets profile.

TypeDirect peer
Description

The subject company itself; included as a reference point given the firmographic name (Retrophin) and operational entity (Travere Therapeutics) refer to the same organization, useful for historical comparisons.

TypeBroad incumbent
Description

Ultragenyx is a rare and ultra-rare disease biopharma with a multi-asset pipeline and similar specialty distribution approach; HCU-adjacent metabolic disease portfolio makes it thematically comparable to Travere's HCU ambition.

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 risks6 records

Each record includes

Headline, Details, Source

Key highlights7 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

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

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 rounds

Each record includes

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

Investors

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 →

Retrophin

Rare Disease Specialty PharmaceuticalsRetrophin.com

Travere Therapeutics (formerly Retrophin) is a publicly traded, San Diego-based biopharmaceutical company developing and commercializing FDA-approved therapies for rare kidney and metabolic diseases including FSGS, IgA Nephropathy, and cystinuria.

What Retrophin does

Retrophin (now operating as Travere Therapeutics, Inc.) is a publicly traded biopharmaceutical company headquartered in San Diego, California, that focuses on developing and commercializing therapies for people living with rare diseases. Founded in 2012 and rebranded from its original Retrophin identity to Travere Therapeutics in 2022, the company is listed on NASDAQ (evidenced by Nasdaq Listing Rule 5635(c)(4) disclosures) and operates across four therapeutic areas: IgA Nephropathy (IgAN), Focal Segmental Glomerulosclerosis (FSGS), Classical Homocystinuria (HCU), and Cystinuria. The company has a stated headcount of 101-250 employees and structures its go-to-market around direct physician and patient outreach, patient advocacy partnerships, and specialty care channels in rare kidney disease communities.

The commercial portfolio centers on FILSPARI (sparsentan), an endothelin angiotensin receptor antagonist that has received full U.S. FDA approval for both FSGS — where it is the first and only approved medicine — and IgA Nephropathy. Travere also markets Thiola and Thiola EC for cystinuria (registered trademarks of Mission Pharmacal Company, held under license or distribution arrangement). The development pipeline is anchored by Pegtibatinase, an investigational enzyme replacement therapy for Classical Homocystinuria, expanding the proprietary science base into rare metabolic disease. Filspari, Total Care Hub, and Travere TotalCare are registered trademarks of Travere Therapeutics.

Revenue is generated through prescription pharmaceutical product sales of FDA-approved therapies (FILSPARI; Thiola / Thiola EC) distributed within the United States via specialty pharmacy channels to healthcare providers and patients. Patient access is supported by branded programs — Total Care Hub and Travere TotalCare — providing adherence and care-coordination services. The company engages the market through a multi-channel model: organic social (Facebook, Instagram, LinkedIn, X, YouTube), content marketing through the Rare Life patient-story program, medical affairs engagement including presentations at major scientific congresses such as the European Renal Association, and earned media / investor relations. Specific drug pricing is not publicly disclosed and is accessed via healthcare providers and specialty pharmacies using standard insurance coverage mechanics.

Retrophin firmographics

Firmographics
Name
Retrophin
Legal name
Travere Therapeutics, Inc.
Website
https://Retrophin.com
Company type
Public
Founded year
2012
Operating status
Operating
Headcount range
101–250 employees
Short description
Travere Therapeutics (formerly Retrophin) is a publicly traded, San Diego-based biopharmaceutical company developing and commercializing FDA-approved therapies for rare kidney and metabolic diseases including FSGS, IgA Nephropathy, and cystinuria.
Ownership category
akta.pro rank

Retrophin industry classification

Industry
Product category
Rare Disease Specialty Pharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Rare Renal & Nephrology Disorder Therapies (HLAIAIAI)
akta.pro secondary industries
Nephrology & Urology Specialty Pharmaceuticals (HLAIACAH), Nephrology & Urology Pharmaceuticals (HLAIAAAM), Genetic & Rare Kidney Disease Clinics (HLAKAHAO)

Keywords

  • Rare disease therapeutics
  • Kidney disease treatments
  • Orphan drug development
  • Specialty pharmaceuticals
  • Enzyme replacement therapy

Where Retrophin is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Retrophin business model

Business model
GTM type
B2B and B2C
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Operations, Supply Chain

Revenue model

  1. Pharmaceutical Product Sales: Revenue generated from the sale of FDA-approved prescription medications including FILSPARI (sparsentan) for FSGS and IgAN, and Thiola/Thiola EC for cystinuria. The company develops and commercializes therapies for rare kidney diseases and metabolic disorders.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Retrophin product offering

Product offering

Core offering

Retrophin (operating as Travere Therapeutics) develops and commercializes FDA-approved prescription therapies for rare kidney diseases and rare metabolic disorders. Core commercial products include FILSPARI (sparsentan) for Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN), and Thiola/Thiola EC for cystinuria. The company's pipeline includes Pegtibatinase, an investigational enzyme replacement therapy for Classical Homocystinuria (HCU).

Product overview

Travere Therapeutics (formerly Retrophin) is a patient-centered biopharmaceutical company focused on developing therapies for rare kidney diseases. The company's product portfolio includes FILSPARI (sparsentan), an FDA-approved treatment for Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN), and Thiola/Thiola EC for cystinuria. The pipeline includes Pegtibatinase for Classical Homocystinuria (HCU). The company operates across four main therapeutic areas: IgA Nephropathy, FSGS, Classical Homocystinuria, and Cystinuria.

Differentiator

Problem solved

Functional benefit

Brands

  • Total Care Hub: Registered trademark; patient support and care program
  • Travere TotalCare
  • Filspari
  • Thiola

Products and services

  • FILSPARI (sparsentan) FILSPARI (sparsentan) is an FDA-approved endothelin angiotensin receptor antagonist indicated for the treatment of Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN). It is the first and only approved medicine for FSGS, targeting patients with rare kidney diseases who have limited therapeutic options.
  • Thiola Thiola is a registered trademark prescription medication for the treatment of cystinuria, a rare metabolic disorder. It is licensed or acquired from Mission Pharmacal Company.
  • Thiola EC Thiola EC is an enteric-coated formulation of the cystinuria treatment medication Thiola, providing an alternative dosing form for patients with cystinuria. Thiola EC is a registered trademark of Mission Pharmacal Company.
  • Pegtibatinase Pegtibatinase is an investigational enzyme replacement therapy in clinical development for the treatment of Classical Homocystinuria (HCU), a rare inherited metabolic disorder.

Companies that use Retrophin

Customer profile

Segments2 records

Ideal customer profiles2 records

Retrophin technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Retrophin partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • European Renal Association (ERA)minorStrategic or Co-development Partner · 4 June 2026Travere Therapeutics presented long-term open-label extension data from the Phase 3 DUPLEX Study at the 63rd European Renal Association (ERA) 2026 Congress, showcasing clinical trial results for their therapeutic candidates.

Scale indicators1 record

Recent moves6 records

Expansion highlights5 records

Retrophin competitors and assessment

Company assessment

Direct peers

  • Calliditas Therapeutics: Calliditas developed Tarpeyo, an FDA-approved targeted-release budesonide for IgA Nephropathy, directly competing with Travere's FILSPARI in the same rare kidney indication and overlapping specialty nephrology customer base.
  • Chinook Therapeutics (Novartis): Pre-acquisition by Novartis, Chinook was a clinical-stage rare kidney disease company developing therapies for IgAN and other rare nephropathies, making it a direct comparator in rare kidney pipeline strategy and indication focus.
  • Vera Therapeutics: Vera is developing atacicept for IgA Nephropathy, positioning it as a direct competitor to FILSPARI in IgAN with a similar specialty nephrology commercial target and patient advocacy model.
  • Reata Pharmaceuticals: Reata developed and commercialized bardoxolone methyl for rare forms of CKD, making it a comparable rare kidney disease biopharma with overlapping nephrology prescribers and similar regulatory pathway focus.
  • Travere Therapeutics (self-reference): The subject company itself; included as a reference point given the firmographic name (Retrophin) and operational entity (Travere Therapeutics) refer to the same organization, useful for historical comparisons.

Broad incumbents

  • Otsuka Pharmaceutical: Otsuka markets tolvaptan for ADPKD, a rare kidney disease, and operates a broad rare disease and specialty pharma portfolio that overlaps with Travere's nephrology focus and specialty pharmacy distribution model.
  • Alexion / AstraZeneca Rare Disease: Alexion is a global rare disease leader with complement-mediated kidney therapies (e.g., Soliris/Ultomiris in aHUS) and overlapping rare disease patient advocacy and specialty distribution infrastructure.
  • BioMarin Pharmaceutical: BioMarin is an established rare disease biopharma with a multi-indication orphan drug portfolio and a similar specialty distribution and patient access model relevant to Travere's commercial approach.
  • Vertex Pharmaceuticals: Vertex is expanding from its rare disease CF franchise into additional rare and specialty indications (including nephrology-adjacent assets via Alpine acquisition), making it a comparable scaling rare disease biopharma with similar capital markets profile.
  • Ultragenyx Pharmaceutical: Ultragenyx is a rare and ultra-rare disease biopharma with a multi-asset pipeline and similar specialty distribution approach; HCU-adjacent metabolic disease portfolio makes it thematically comparable to Travere's HCU ambition.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Retrophin social profiles

Digital presence

Retrophin financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Retrophin leadership team

Management profile

Number of profiles

Profiles1 record

Retrophin funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Retrophin 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 Retrophin

What does Retrophin do?

Retrophin (operating as Travere Therapeutics) develops and commercializes FDA-approved prescription therapies for rare kidney diseases and rare metabolic disorders. Core commercial products include FILSPARI (sparsentan) for Focal Segmental Glomerulosclerosis (FSGS) and IgA Nephropathy (IgAN), and Thiola/Thiola EC for cystinuria. The company's pipeline includes Pegtibatinase, an investigational enzyme replacement therapy for Classical Homocystinuria (HCU).

Is Retrophin a public or private company?

Retrophin is a public company. It is classified as public and is currently operating.

When was Retrophin founded?

Retrophin was founded in 2012. It employs 101 to 250 people.

Where is Retrophin based?

Retrophin is headquartered in San Diego, United States, in the North America region.

How does Retrophin make money?

One revenue line is on record: pharmaceutical Product Sales.

Who are Retrophin's main competitors?

Direct peers on record are Calliditas Therapeutics, Chinook Therapeutics (Novartis), Vera Therapeutics, Reata Pharmaceuticals and Travere Therapeutics (self-reference). Broad incumbents are Otsuka Pharmaceutical, Alexion / AstraZeneca Rare Disease, BioMarin Pharmaceutical, Vertex Pharmaceuticals and Ultragenyx Pharmaceutical.

Does Retrophin have an API?

No public API is recorded for Retrophin.

What industry is Retrophin in?

Retrophin's product category is Rare Disease Specialty Pharmaceuticals. Its primary akta.pro industry code is HLAIAIAI, Rare Renal & Nephrology Disorder Therapies, with a secondary code of HLAIACAH, Nephrology & Urology Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
BenzingaThe Daily Biotech Pulse: Gilead Gets Full Approval For Remdesivir, Akebia's Positive Readout, Foghorn IPOGilead Sciences received full FDA approval for its antiviral drug Veklury (remdesivir) to treat hospitalized COVID-19 patients, causing its stock to rise 7.1%. In other developments, Retrophin Inc announced an agreement to acquire Orphan Technologies Limited for up to $517 million to obtain the enzyme replacement therapy OT-58.GlobeNewswireRetrophin, Inc. Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)Retrophin granted inducement equity grants to four new employees on October 10, 2020, covering 58,750 shares total. The grants include 37,500 stock options and 21,250 restricted stock units, with options priced at $20.68 per share and vesting over four years.PR NewswireNORD Highlights New Era of Innovation and Public Health Awareness in Virtual 2020 Rare Diseases and Orphan Products Breakthrough SummitThe National Organization for Rare Disorders (NORD) virtually hosted its 2020 Rare Diseases and Orphan Products Breakthrough Summit on October 8-9, marking the first time the organization presented its annual conference exclusively online, with nearly 900 registrants from more than 20 countries gathering to discuss rare disease innovation and public health. FDA Commissioner Stephen Hahn delivered a keynote highlighting 51 orphan indications approved by the agency through July 2020, while day one featured breakout sessions on topics including gene therapy, orphan drug development, and diagnostic testing access. The event, themed "Entering a New Era," was sponsored by Eversana, Insmed, Retrophin, and Takeda, and concluded with the Rare Impact Awards celebrating contributions to the rare disease community.PR NewswireExperimental Drug More Effective in Treating Rare Kidney DiseaseA phase II clinical trial published in the Journal of the American Society of Nephrology found that the experimental drug sparsentan reduced proteinuria by 45% in patients with focal segmental glomerulosclerosis (FSGS), more than twice the 19% reduction seen with the standard treatment irbesartan. The trial enrolled 109 patients across 44 sites in the US and Europe over eight weeks, with sparsentan showing minimal serious side effects. The drug, manufactured by Retrophin, Inc., could become the first approved therapy for FSGS, a rare kidney disease affecting up to 40,000 people in the US with no currently approved treatments.GlobeNewswireRetrophin and Censa Pharmaceuticals Enter into Strategic Collaboration to Advance CNSA-001 for the Treatment of Phenylketonuria (PKU)Retrophin and Censa Pharmaceuticals entered a joint development agreement to evaluate CNSA-001 for phenylketonuria, with Retrophin paying $10 million upfront. The Phase 2 proof-of-concept study is expected to commence in mid-2018, and Retrophin holds an exclusive option to acquire Censa pending positive results.Business InsiderThe life of 'Pharma bro' Martin Shkreli, who was convicted of securities fraud and faces up to 20 years in prisonMartin Shkreli was found guilty of three counts of securities fraud on August 4, 2017, and faces up to 20 years in prison. He was acquitted on a key charge of looting Retrophin to pay hedge fund debts. The verdict followed his conviction after a trial that ended with him claiming innocence on the most important charges.CNBCMartin Shkreli's lawyer and 'cowboy' venture capitalist duel over what horses and investments are worthDuring Martin Shkreli's federal securities fraud trial, investor Darren Blanton, who claims to have been defrauded by Shkreli, hesitated to disclose his net worth while being cross-examined. Despite claiming ownership of valuable horse assets, Blanton suggested that their worth is subjective and tied to market conditions, indicating a complex financial situation with his investments. Blanton's interactions with Shkreli and his testimony shed light on the controversies surrounding investments in Shkreli's hedge funds and his company Retrophin.PR NewswireImprimis Pharmaceuticals Begins Dispensing Lower Cost Alternative to Thiola®Imprimis Pharmaceuticals announced the availability of new patent-pending customizable delayed-release tiopronin formulations as a lower-cost therapeutic alternative to FDA-approved Thiola for cystinuria patients. The compounded formulations offer at least 60% cost reduction compared to Thiola and may significantly reduce the number of pills patients need to take daily for this chronic genetic kidney stone condition. The development addresses access concerns stemming from a 2,000% price increase by Retrophin that has burdened the estimated 4,000 to 5,000 U.S. patients who are candidates for tiopronin treatment.GlobeNewswireRetrophin to Present at the Barclays Global Healthcare ConferenceRetrophin's CEO Stephen Aselage will present at the Barclays Global Healthcare Conference in Miami on March 17, 2016. The company's pipeline includes sparsentan for FSGS and RE-024 for PKAN, with revenues from marketed products Chenodal, Cholbam, and Thiola.Business InsiderHere's what's happened to the companies Martin Shkreli used to runMartin Shkreli's former companies have diverged: Turing Pharmaceuticals kept its Daraprim price hike, Retrophin retained its Thiola price increase, and KaloBios filed for bankruptcy after Shkreli's arrest. The hedge funds he managed are also mentioned, with one involved in SEC fraud charges.