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LIB Therapeutics

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uuid000cbxs

Namestring
LIB Therapeutics
Legal namestring
LIB Therapeutics, Inc.
Company typeenum
Private
Founded yearint
2015
Descriptiontext

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company founded in 2015 and headquartered in Cincinnati, Ohio. The company develops and commercializes LEROCHOL (lerodalcibep-liga), a third-generation PCSK9 inhibitor approved by the FDA in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. The product's anti-PCSK9 binding domain is an 11-kDa adnectin polypeptide fused to human serum albumin, differentiating it from monoclonal antibody-based PCSK9 inhibitors (Repatha, Praluent) and siRNA therapies (Leqvio). LEROCHOL is administered as a once-monthly subcutaneous injection with a small injection volume and extended room-temperature stability of up to three months, with sustained LDL-C reductions of approximately 50-60% demonstrated across the Phase 3 LIBerate program of over 2,900 patients.

The company operates a hybrid commercial model combining direct-to-patient cash-pay sales at $199/month through LEROCHOL.com with traditional healthcare-provider prescription distribution. Geographic expansion is advancing through an EMA Marketing Authorization Application with anticipated 2H 2026 approval, a Greater China Biologics License Application expected 1H 2026 via an exclusive partnership with Everest Medicines (succeeding the original $325M Hasten Biopharmaceutical collaboration), and pursuit of additional EU regional partners. The company is led by a credentialed team including CEO David Cory (former Eiger BioPharmaceuticals CEO, co-founder of CoTherix) and Founder/Chief Executive & Scientific Officer Dr. Evan Stein, supported by senior commercial and operational leadership hired in 2024-2026 to scale the US launch and ex-US regulatory strategy.

Short descriptiontext

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company that develops LEROCHOL, a once-monthly third-generation PCSK9 inhibitor FDA-approved in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, marketed direct-to-patient at $199/month.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersCincinnati, United States
HQ citystring
Cincinnati
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
PCSK9 inhibitors, lipid lowering therapy, cardiovascular therapeutics, LDL cholesterol treatment, biopharmaceutical products
Industry2 codes
1Preventive Cardiology & Lipidology
CodeHLAKABAFPrimaryYes
2Chronic Disease Management Pathways (e.g., diabetes, CHF, COPD)
CodeHLACAGAGPrimaryNo
NAICS code1 code
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Cardiovascular Pharmaceuticals
Social media profiles1 record
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeSubscription Recurring
Description

Direct-to-patient cash-pay sales of LEROCHOL at $199/month with prefilled syringe and auto-injector formulations. Revenue also generated through payer reimbursement and insurance coverage for prescriptions written by healthcare providers.

libtherapeutics.com
2Licensing Royalties (Greater China)
TypeLicensing Royalties
Description

Everest Medicines holds exclusive license to develop, register and commercialize LEROCHOL in Greater China. LIB Therapeutics receives licensing revenue and royalties from this territory under the $325M strategic collaboration with Hasten Biopharmaceutical.

libtherapeutics.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Supply Chain, Operations, Marketing or Sales
Pricing details1 tier
1Monthly cash-pay subscription at $199/month
ModelSubscriptionBilling cadenceMonthly
Notes

LEROCHOL 300mg/1.2mL injection available for $199/month via direct-to-patient cash-pay option. This is positioned as a substantial discount to other PCSK9 inhibitors' direct-to-patient cash prices. Prefilled syringe available now; auto-injector pen expected later in 2026.

libtherapeutics.com
GTM typeB2B and B2C
B2B and B2C
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1LEROCHOL
Description

Brand name for the company's FDA-approved drug lerodalcibep-liga, a third-generation PCSK9 inhibitor for lowering LDL cholesterol in adults with hypercholesterolemia.

libtherapeutics.com
Core offering1 text field

LIB Therapeutics develops and commercializes LEROCHOL (lerodalcibep-liga), a third-generation PCSK9 inhibitor administered as a once-monthly, small-volume subcutaneous injection for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. The product uses a proprietary adnectin-based protein-binding technology with extended room-temperature stability and is sold via a direct-to-patient cash-pay model at $199/month alongside traditional prescription-based distribution.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 9 values shown
  • 52% mean LDL-C reduction through 124 weeks (2.3 mmol/L absolute reduction)
+8 more records
Product overview1 text field

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company with a single focused product: LEROCHOL (lerodalcibep-liga). LEROCHOL is a third-generation PCSK9 inhibitor approved by the FDA in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. It is administered as a once-monthly subcutaneous injection with extended room-temperature stability. The company is pursuing additional regulatory approvals in Europe (EMA MAA submitted) and Greater China (BLA expected 1H 2026).

Product and service2 records
1LEROCHOL (lerodalcibep-liga) Pre-filled Syringe
CategoryCardiovascular Pharmaceuticals
Description

A third-generation PCSK9 inhibitor administered as a once-monthly, single small-volume subcutaneous injection for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. Available via direct-to-patient cash-pay subscription at $199/month through LEROCHOL.com and via traditional prescription with payer reimbursement.

2LEROCHOL (lerodalcibep-liga) Auto-Injector Pen
CategoryCardiovascular Pharmaceuticals
Description

Auto-injector pen formulation of LEROCHOL for patient self-administration of once-monthly subcutaneous PCSK9 inhibitor therapy. Expected to launch later in 2026.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-12-01
Description

Everest Medicines (HKEX 1952.HK) holds exclusive license to develop, register and commercialize LEROCHOL in Greater China. Everest entered into strategic agreement with Hasten Biopharmaceutical and LIB Therapeutics in December 2025. Everest focuses on discovering, developing, manufacturing and commercializing transformative pharmaceutical products for Asian markets.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-09-12
Description

$325 million strategic collaboration announced September 12, 2023 to develop and commercialize lerodalcibep in Greater China. Hasten obtained rights to develop and commercialize lerodalcibep and is responsible for regulatory approval in these territories. Everest Medicines subsequently entered into strategic agreement with Hasten in December 2025 to license LEROCHOL in Greater China.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Peers8 records
TypeDirect peer
Description

Novartis acquired The Medicines Company to commercialize Leqvio (inclisiran), a siRNA PCSK9-targeted therapy administered twice yearly. Leqvio is the most differentiated direct competitor offering an alternative mechanism and longer dosing interval compared to lerodalcibep.

TypeOthers
Description

Ionis Pharmaceuticals originated the antisense and siRNA chemistries behind Leqvio's PCSK9 mechanism and continues to develop lipid-targeting nucleic acid therapies. Ionis is comparable as a developer of PCSK9/LDL-C targeted therapeutics with similar lipid biology expertise.

TypeEmerging player
Description

Verve Therapeutics is developing in vivo gene-editing therapies targeting PCSK9 for one-and-done LDL-C reduction. Its PCSK9 gene-editing approach targets the same biological pathway as LEROCHOL and represents a potential future disruptive therapy.

TypeDirect peer
Description

Esperion markets bempedoic acid for LDL-C lowering in statin-intolerant patients. While targeting a different mechanism, Esperion competes in the same prescriber workflow as adjunct lipid-lowering therapy for ASCVD patients who fail to achieve LDL-C goals on statins.

TypeRegional player
Description

Madrigal commercializes Rezdiffra for MASH (liver disease) but operates in the cardiometabolic space and competes for cardiovascular-metabolic prescriber attention. Comparable as a recently-launched specialty cardiometabolic drug company with a single approved product.

TypeDirect peer
Description

Amgen markets Repatha, the first FDA-approved PCSK9 monoclonal antibody inhibitor for LDL-C reduction. Repatha is the direct head-to-head competitor to LEROCHOL in the same indication (hypercholesterolemia, HeFH, ASCVD), creating the central competitive dynamic LIB Therapeutics must navigate.

TypeEmerging player
Description

NewAmsterdam Pharma is developing obicetrapib, a next-generation CETP inhibitor for LDL-C lowering. It is in late-stage Phase 3 trials and would enter the same adjunct-to-statin market space that LEROCHOL targets for ASCVD and FH patients.

TypeDirect peer
Description

Regeneron and Sanofi jointly commercialize Praluent, the second approved monoclonal antibody PCSK9 inhibitor in the same market segment. Praluent competes directly on efficacy, dosing, and formulary positioning for hypercholesterolemia and ASCVD patients.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

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
Profiles14 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 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 →

LIB Therapeutics

Cardiovascular Pharmaceuticalslibtherapeutics.com

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company that develops LEROCHOL, a once-monthly third-generation PCSK9 inhibitor FDA-approved in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, marketed direct-to-patient at $199/month.

What LIB Therapeutics does

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company founded in 2015 and headquartered in Cincinnati, Ohio. The company develops and commercializes LEROCHOL (lerodalcibep-liga), a third-generation PCSK9 inhibitor approved by the FDA in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. The product's anti-PCSK9 binding domain is an 11-kDa adnectin polypeptide fused to human serum albumin, differentiating it from monoclonal antibody-based PCSK9 inhibitors (Repatha, Praluent) and siRNA therapies (Leqvio). LEROCHOL is administered as a once-monthly subcutaneous injection with a small injection volume and extended room-temperature stability of up to three months, with sustained LDL-C reductions of approximately 50-60% demonstrated across the Phase 3 LIBerate program of over 2,900 patients.

The company operates a hybrid commercial model combining direct-to-patient cash-pay sales at $199/month through LEROCHOL.com with traditional healthcare-provider prescription distribution. Geographic expansion is advancing through an EMA Marketing Authorization Application with anticipated 2H 2026 approval, a Greater China Biologics License Application expected 1H 2026 via an exclusive partnership with Everest Medicines (succeeding the original $325M Hasten Biopharmaceutical collaboration), and pursuit of additional EU regional partners. The company is led by a credentialed team including CEO David Cory (former Eiger BioPharmaceuticals CEO, co-founder of CoTherix) and Founder/Chief Executive & Scientific Officer Dr. Evan Stein, supported by senior commercial and operational leadership hired in 2024-2026 to scale the US launch and ex-US regulatory strategy.

LIB Therapeutics firmographics

Firmographics
Name
LIB Therapeutics
Legal name
LIB Therapeutics, Inc.
Website
https://libtherapeutics.com
Company type
Private
Founded year
2015
Operating status
Operating
Headcount range
1–10 employees
Short description
LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company that develops LEROCHOL, a once-monthly third-generation PCSK9 inhibitor FDA-approved in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, marketed direct-to-patient at $199/month.
Ownership category
akta.pro rank

LIB Therapeutics industry classification

Industry
Product category
Cardiovascular Pharmaceuticals
NAICS
Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Preventive Cardiology & Lipidology (HLAKABAF)
akta.pro secondary industry
Chronic Disease Management Pathways (e.g., diabetes, CHF, COPD) (HLACAGAG)

Keywords

  • PCSK9 inhibitors
  • Lipid lowering therapy
  • Cardiovascular therapeutics
  • LDL cholesterol treatment
  • Biopharmaceutical products

Where LIB Therapeutics is headquartered

Location

Headquarters

HQ city
Cincinnati
HQ country
United States
HQ region
North America

Offices1 record

Markets served

LIB Therapeutics business model

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

Revenue model

  1. Pharmaceutical Product Sales: Direct-to-patient cash-pay sales of LEROCHOL at $199/month with prefilled syringe and auto-injector formulations. Revenue also generated through payer reimbursement and insurance coverage for prescriptions written by healthcare providers.
  2. Licensing Royalties (Greater China): Everest Medicines holds exclusive license to develop, register and commercialize LEROCHOL in Greater China. LIB Therapeutics receives licensing revenue and royalties from this territory under the $325M strategic collaboration with Hasten Biopharmaceutical.

Pricing tiers

ModelBillingPrice
SubscriptionMonthlyMonthly cash-pay subscription at $199/month

Go-to-market motion3 records

Distribution channels4 records

Marketing channels4 records

LIB Therapeutics product offering

Product offering

Core offering

LIB Therapeutics develops and commercializes LEROCHOL (lerodalcibep-liga), a third-generation PCSK9 inhibitor administered as a once-monthly, small-volume subcutaneous injection for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. The product uses a proprietary adnectin-based protein-binding technology with extended room-temperature stability and is sold via a direct-to-patient cash-pay model at $199/month alongside traditional prescription-based distribution.

Product overview

LIB Therapeutics is a privately held, commercial-stage biopharmaceutical company with a single focused product: LEROCHOL (lerodalcibep-liga). LEROCHOL is a third-generation PCSK9 inhibitor approved by the FDA in December 2025 for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. It is administered as a once-monthly subcutaneous injection with extended room-temperature stability. The company is pursuing additional regulatory approvals in Europe (EMA MAA submitted) and Greater China (BLA expected 1H 2026).

Differentiator

Problem solved

Functional benefit

Brands

  • LEROCHOL: Brand name for the company's FDA-approved drug lerodalcibep-liga, a third-generation PCSK9 inhibitor for lowering LDL cholesterol in adults with hypercholesterolemia.

Products and services

  • LEROCHOL (lerodalcibep-liga) Pre-filled Syringe A third-generation PCSK9 inhibitor administered as a once-monthly, single small-volume subcutaneous injection for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. Available via direct-to-patient cash-pay subscription at $199/month through LEROCHOL.com and via traditional prescription with payer reimbursement.
  • LEROCHOL (lerodalcibep-liga) Auto-Injector Pen Auto-injector pen formulation of LEROCHOL for patient self-administration of once-monthly subcutaneous PCSK9 inhibitor therapy. Expected to launch later in 2026.

Quantifiable outcome

  • 52% mean LDL-C reduction through 124 weeks (2.3 mmol/L absolute reduction)
  • +8 more outcomes

Companies that use LIB Therapeutics

Customer profile

Segments4 records

Ideal customer profiles2 records

LIB Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

LIB Therapeutics partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • Everest MedicinescoreChannel Partner/ Reseller/ Distributor · 1 December 2025Everest Medicines (HKEX 1952.HK) holds exclusive license to develop, register and commercialize LEROCHOL in Greater China. Everest entered into strategic agreement with Hasten Biopharmaceutical and LIB Therapeutics in December 2025. Everest focuses on discovering, developing, manufacturing and commercializing transformative pharmaceutical products for Asian markets.
  • Hasten Biopharmaceutical Co., Ltd.coreStrategic or Co-development Partner · 12 September 2023$325 million strategic collaboration announced September 12, 2023 to develop and commercialize lerodalcibep in Greater China. Hasten obtained rights to develop and commercialize lerodalcibep and is responsible for regulatory approval in these territories. Everest Medicines subsequently entered into strategic agreement with Hasten in December 2025 to license LEROCHOL in Greater China.

Scale indicators9 records

Recent moves6 records

LIB Therapeutics competitors and assessment

Company assessment

Direct peers

  • Novartis (Leqvio/inclisiran): Novartis acquired The Medicines Company to commercialize Leqvio (inclisiran), a siRNA PCSK9-targeted therapy administered twice yearly. Leqvio is the most differentiated direct competitor offering an alternative mechanism and longer dosing interval compared to lerodalcibep.
  • Esperion Therapeutics (Nexletol/Nexlizet): Esperion markets bempedoic acid for LDL-C lowering in statin-intolerant patients. While targeting a different mechanism, Esperion competes in the same prescriber workflow as adjunct lipid-lowering therapy for ASCVD patients who fail to achieve LDL-C goals on statins.
  • Amgen (Repatha/evolocumab): Amgen markets Repatha, the first FDA-approved PCSK9 monoclonal antibody inhibitor for LDL-C reduction. Repatha is the direct head-to-head competitor to LEROCHOL in the same indication (hypercholesterolemia, HeFH, ASCVD), creating the central competitive dynamic LIB Therapeutics must navigate.
  • Regeneron / Sanofi (Praluent/alirocumab): Regeneron and Sanofi jointly commercialize Praluent, the second approved monoclonal antibody PCSK9 inhibitor in the same market segment. Praluent competes directly on efficacy, dosing, and formulary positioning for hypercholesterolemia and ASCVD patients.

Others

  • Ionis Pharmaceuticals: Ionis Pharmaceuticals originated the antisense and siRNA chemistries behind Leqvio's PCSK9 mechanism and continues to develop lipid-targeting nucleic acid therapies. Ionis is comparable as a developer of PCSK9/LDL-C targeted therapeutics with similar lipid biology expertise.

Emerging players

  • Verve Therapeutics: Verve Therapeutics is developing in vivo gene-editing therapies targeting PCSK9 for one-and-done LDL-C reduction. Its PCSK9 gene-editing approach targets the same biological pathway as LEROCHOL and represents a potential future disruptive therapy.
  • NewAmsterdam Pharma (obicetrapib): NewAmsterdam Pharma is developing obicetrapib, a next-generation CETP inhibitor for LDL-C lowering. It is in late-stage Phase 3 trials and would enter the same adjunct-to-statin market space that LEROCHOL targets for ASCVD and FH patients.

Regional players

  • Madrigal Pharmaceuticals: Madrigal commercializes Rezdiffra for MASH (liver disease) but operates in the cardiometabolic space and competes for cardiovascular-metabolic prescriber attention. Comparable as a recently-launched specialty cardiometabolic drug company with a single approved product.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

LIB Therapeutics social profiles

Digital presence

LIB Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

LIB Therapeutics leadership team

Management profile

Number of profiles

Profiles14 records

LIB Therapeutics funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

LIB Therapeutics 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 LIB Therapeutics

What does LIB Therapeutics do?

LIB Therapeutics develops and commercializes LEROCHOL (lerodalcibep-liga), a third-generation PCSK9 inhibitor administered as a once-monthly, small-volume subcutaneous injection for reducing LDL cholesterol in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. The product uses a proprietary adnectin-based protein-binding technology with extended room-temperature stability and is sold via a direct-to-patient cash-pay model at $199/month alongside traditional prescription-based distribution.

Is LIB Therapeutics a public or private company?

LIB Therapeutics is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was LIB Therapeutics founded?

LIB Therapeutics was founded in 2015. It employs 1 to 10 people.

Where is LIB Therapeutics based?

LIB Therapeutics is headquartered in Cincinnati, United States, in the North America region.

How does LIB Therapeutics make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are licensing Royalties (Greater China).

Who are LIB Therapeutics's main competitors?

Direct peers on record are Novartis (Leqvio/inclisiran), Esperion Therapeutics (Nexletol/Nexlizet), Amgen (Repatha/evolocumab) and Regeneron / Sanofi (Praluent/alirocumab). Ionis Pharmaceuticals is listed as an others. Emerging players are Verve Therapeutics and NewAmsterdam Pharma (obicetrapib). Madrigal Pharmaceuticals is listed as a regional player.

Does LIB Therapeutics have an API?

No public API is recorded for LIB Therapeutics.

What industry is LIB Therapeutics in?

LIB Therapeutics's product category is Cardiovascular Pharmaceuticals. Its primary akta.pro industry code is HLAKABAF, Preventive Cardiology & Lipidology, with a secondary code of HLACAGAG, Chronic Disease Management Pathways (e.g., diabetes, CHF, COPD). Its NAICS code is 5417 and its SIC code is 8731.

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Live signals
The HinduSun Pharma inks pact with LIB Therapeutics to sell LDL-C drugSun Pharma and LIB Therapeutics announced an exclusive licensing agreement for lerodalcibep, a PCSK9 inhibitor, outside the U.S. and China. The PCSK9 inhibitor market outside those regions reached $3.7 billion in Q2 2026, with Europe accounting for $2.9 billion. Sun Pharma will pursue regulatory approvals in licensed territories.NDTV ProfitSun Pharma To Commercialise Novel Bad Cholesterol Drug Lerodalcibep In Ex-US, China MarketsSun Pharma secured exclusive rights to commercialize and manufacture lerodalcibep, a PCSK9 inhibitor, outside the US and China. The deal covers a $3.7 billion market outside those regions, with LIB Therapeutics receiving upfront and milestone payments. Sun Pharma will seek regulatory approvals in territories where the drug is not yet cleared.NDTV ProfitSun Pharma To Commercialise Novel Bad Cholesterol Drug Lerodalcibep In Ex-US, China MarketsSun Pharma secured exclusive rights to commercialize lerodalcibep outside the US and China, with LIB Therapeutics receiving upfront and milestone payments. The drug, a monthly PCSK9 inhibitor, received EU approval and targets a $3.7 billion market outside those regions. Sun Pharma will seek regulatory approvals in territories where the drug is not yet cleared.Business Wire BlogLIB Therapeutics and Sun Pharma Announce Global Licensing, Commercialization and Manufacturing Agreement for Lerodalcibep, a Novel PCSK9 Inhibitor, Ex-US and China; Lerodalcibep (Lyrokaul®) Approved iSun Pharma and LIB Therapeutics announced an exclusive licensing agreement for lerodalcibep (LEROCHOL) outside the US and China, with Sun Pharma commercializing and manufacturing. The drug received EU approval on September 21, 2026, and LIB will receive upfront and milestone payments plus royalties. LIB plans to launch the autoinjector in the US by January 2027.The Times of IndiaSun Pharma signs major deal with LIB Therapeutics of USSun Pharma signed an exclusive deal with US-based LIB Therapeutics for the manufacture, commercialization, and global licensing of Lerodalcibep, a PCSK9 inhibitor, across all markets except the US and China. The drug, marketed as Lyrokaul in Europe, will generate upfront and milestone payments plus royalties, with the PCSK9 market outside those two countries valued at $3.7 billion.The Times of IndiaSun Pharma steps into PCSK9 arena with LIB Therapeutics’ monthly-shotSun Pharma acquired exclusive rights to manufacture and market LIB Therapeutics' PCSK9 inhibitor Lyrokaul in ex-US and China. The deal targets a $3.7 billion market growing at 38% CAGR, with LIB receiving undisclosed upfront, milestone, and royalty payments. Sun Pharma will pursue regulatory approvals in licensed territories.The Times of IndiaSun Pharma signs major deal with LIB Therapeutics of US, gains access to $3.7-bn global market for bad cholesterol inhibitor PCSK9Sun Pharma signed a deal with LIB Therapeutics for the PCSK9 inhibitor Lerodalcibep, gaining access to a $3.7 billion global market outside the US and China. The drug received EU and US approvals, and Sun Pharma will handle regulatory clearances in licensed markets.BusinessLineSun Pharma inks global licensing pact with LIB Therapeutics for cholesterol drug LerodalcibepSun Pharma signed an exclusive agreement with LIB Therapeutics to manufacture, commercialize, and globally license Lerodalcibep outside the US and China. The deal includes upfront and milestone payments plus royalties, targeting a $3.7-billion PCSK9 market growing at 38% CAGR. Sun Pharma will pursue regulatory approvals in licensed territories.Business StandardSun Pharma bags rights to $3.7 billion cholesterol drug market globallySun Pharma signed a global licensing deal with LIB Therapeutics for Lerodalcibep, a once-monthly PCSK9 inhibitor, gaining exclusive rights outside the US and China. The deal targets a $3.7 billion market, with Europe accounting for $2.9 billion, and LIB will receive upfront, milestone, and royalty payments.Business StandardSun Pharma signs exclusive licensing agreement with LIB Therapeutics Inc.Sun Pharma and LIB Therapeutics signed an exclusive licensing agreement for lerodalcibep (Lyrokaul) worldwide, excluding the US and China. The deal gives Sun Pharma access to a US$3.7 billion PCSK9 market outside those regions, with LIB receiving upfront and milestone payments plus royalties. Sun Pharma will pursue regulatory approvals in licensed territories.