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Rein Therapeutics

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uuid0003uer

Namestring
Rein Therapeutics
Legal namestring
Rein Therapeutics, Inc.
Websiteurl
reintx.com
Company typeenum
Public
Founded yearint
2013
Descriptiontext

Rein Therapeutics is a clinical-stage biopharmaceutical company headquartered in Austin, Texas, publicly traded on NASDAQ under ticker RNTX. The company develops first-in-class peptide therapeutics for orphan pulmonary and fibrosis indications, with its lead candidate LTI-03 targeting idiopathic pulmonary fibrosis (IPF) — a progressive, fatal lung disease with median survival of 2–4 years and limited therapeutic options. The company originated as Lung Therapeutics in 2013, was acquired by Aileron Therapeutics in October 2023 (transitioning to public listing), and rebranded to Rein Therapeutics in 2025 to reflect its focus on controlling fibrosis.

The core technology centers on a synthetic peptide derived from the Caveolin-1 scaffolding domain (CSD) — a seven-amino-acid sequence that regulates lung repair and cellular movement. LTI-03, the lead asset, employs a dual mechanism of action: anti-fibrotic activity (modulating signaling pathways to inhibit fibroblast activation and tissue scarring) and regenerative activity (protecting alveolar epithelial cells essential for lung function). It is delivered via a dry powder inhaler for direct-to-lung treatment, offering localized delivery with reduced systemic side effects. Two earlier-stage assets round out the pipeline: LTI-01, a proenzyme (zymogen) for loculated pleural effusion that enzymatically breaks down fibrous scar tissue, and LTI-05 for cystic fibrosis.

As a pre-revenue company, Rein Therapeutics has no commercially approved products and generates no operating revenue; its enterprise value is entirely contingent on clinical milestones and pipeline progression. The company funds operations through equity raises, most recently completing a $57.5 million underwritten public offering in May 2026 expected to fund operations into Q1 2028. Its GTM strategy centers on generating clinical data from the Phase 2 RENEW trial (approximately 120 patients across up to 50 sites in five countries) to support FDA and EMA approvals. Upon regulatory approval, the company would distribute through specialty pharmacy and hospital formulary channels.

Short descriptiontext

Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class Caveolin-1-derived peptide therapeutics for orphan pulmonary and fibrosis indications, with lead candidate LTI-03 in Phase 2 for idiopathic pulmonary fibrosis and earlier-stage pipeline assets for pleural effusion and cystic fibrosis.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersAustin, United States
HQ citystring
Austin
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
pulmonary fibrosis treatments, orphan pulmonary disease, fibrosis drug development, respiratory therapeutics, inhaled peptide therapy
Industry2 codes
1Pulmonary Hypertension & Rare Pulmonary Disease Therapies
CodeHLAIAIAGPrimaryYes
2Therapeutic Peptides & Protein/Peptide Biologics
CodeHLAAAAAHPrimaryNo
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Pulmonary Fibrosis Therapeutics
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Drug Development and Commercialization
TypeOne Time License
Description

Pre-revenue clinical-stage biopharmaceutical company developing first-in-class medicines for orphan pulmonary and fibrosis indications. Revenue will come from product sales upon regulatory approval of LTI-03 (IPF), LTI-01 (LPE), and LTI-05 (Cystic fibrosis).

reintx.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

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

Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class synthetic peptide drug candidates for orphan pulmonary and fibrosis indications. Its lead product, LTI-03, is a synthetic peptide derived from Caveolin-1 delivered via dry powder inhaler for the treatment of idiopathic pulmonary fibrosis (IPF), combining anti-fibrotic and regenerative mechanisms of action. The pipeline also includes LTI-01 for loculated pleural effusion and LTI-05 for cystic fibrosis.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • LTI-03 was well tolerated and showed biological activity including reductions in fibrosis biomarkers and preservation of lung repair cells in Phase 1 dose-escalation study
+2 more records
Product overview1 text field

Rein Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of first-in-class multi-pathway treatments for orphan pulmonary and fibrosis indications. The portfolio consists of three main products: LTI-03 (lead product, Phase 2 for idiopathic pulmonary fibrosis via dry powder inhaler), LTI-01 (preclinical/Phase 1 for loculated pleural effusion), and LTI-05 (preclinical for cystic fibrosis). LTI-03 is the primary focus, targeting both anti-fibrotic and regenerative pathways through a novel Caveolin-1 derived peptide mechanism.

Product and service3 records
1LTI-03
CategoryCore Product - Pulmonary Fibrosis Drug Candidate
Description

First-in-class synthetic peptide derived from Caveolin-1 for the treatment of idiopathic pulmonary fibrosis (IPF). Delivered via dry powder inhaler with dual mechanism of action combining anti-fibrotic effects (inhibiting fibroblast activation and tissue scarring) and regenerative effects (protecting epithelial cells essential for lung function). Currently in Phase 2 RENEW clinical trial.

2LTI-01
CategoryPipeline Product - Pleural Effusion Drug Candidate
Description

Proenzyme (zymogen) treatment candidate for loculated pleural effusion (LPE), positioned as the first therapy specifically developed for non-draining LPE. Breaks down fibrous tissue, clearing scarred areas and promoting fluid drainage. Currently in preclinical/Phase 1 development.

3LTI-05
CategoryPipeline Product - Cystic Fibrosis Drug Candidate
Description

Treatment candidate for cystic fibrosis as part of Rein's multi-pathway fibrotic treatments pipeline addressing orphan pulmonary indications. Currently in preclinical development.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biopharma developing integrin-targeting therapies for IPF (bexotegrast/PLN-74809) and other fibrotic diseases. Closest direct peer — same indication, similar Phase 2/3 stage, comparable size and orphan-pulmonary focus.

TypeDirect peer
Description

Developed pamrevlumab (anti-CTGF) for IPF. Direct comparator in IPF fibrosis drug development with similar clinical-stage positioning and biology-driven approach to fibrotic disease.

TypeDirect peer
Description

Small clinical-stage biopharma with an inflammation/fibrosis pipeline (formerly Cerecor). Comparable in scale and stage to Rein, focused on immunology and rare pulmonary indications.

TypeBroad incumbent
Description

Commercial-stage respiratory biopharma with Tyvaso DPI approved for PAH and PH-ILD, adjacent to IPF. A potential strategic acquirer or commercial partner given its established inhaled pulmonary franchise.

TypeBroad incumbent
Description

Markets Ofev (nintedanib), one of two FDA-approved IPF therapies. Sets the standard-of-care bar Rein must clear and is a likely strategic acquirer given its deep respiratory/fibrosis commercial footprint.

TypeBroad incumbent
Description

Markets Esbriet (pirfenidone), the other FDA-approved IPF therapy. Like Boehringer, defines the incumbent treatment paradigm and is a credible strategic acquirer for novel fibrosis mechanisms.

TypeBroad incumbent
Description

Had an IPF program (ziritaxestat) discontinued in Phase 3, illustrating both the strategic interest and the high failure rate in fibrosis drug development. Mid-cap European biopharma with adjacent inflammation/fibrosis R&D.

TypeEmerging player
Description

Clinical-stage biopharma with fibrosis and inflammation pipeline programs. Comparable in scale and clinical-stage orphan disease focus, with similar platform-based approach to novel mechanisms.

TypeBroad incumbent
Description

Large biopharma that has invested in IPF/fibrosis through pipeline deals and is a potential strategic acquirer for novel inhaled fibrosis therapies. Sets competitive benchmark for late-stage clinical and commercial resources.

TypeEmerging player
Description

Small-cap clinical-stage biopharma of similar size, employee count, and NASDAQ-listed profile to Rein Therapeutics, providing a useful comparable for valuation, capital structure, and clinical-stage biotech dynamics.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 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

Segment3 records

Each record includes

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

Ideal customer profile2 records

Each record includes

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

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 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 rounds13 records

Each record includes

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

Investors17 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 →

Rein Therapeutics

Pulmonary Fibrosis Therapeuticsreintx.com

Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class Caveolin-1-derived peptide therapeutics for orphan pulmonary and fibrosis indications, with lead candidate LTI-03 in Phase 2 for idiopathic pulmonary fibrosis and earlier-stage pipeline assets for pleural effusion and cystic fibrosis.

What Rein Therapeutics does

Rein Therapeutics is a clinical-stage biopharmaceutical company headquartered in Austin, Texas, publicly traded on NASDAQ under ticker RNTX. The company develops first-in-class peptide therapeutics for orphan pulmonary and fibrosis indications, with its lead candidate LTI-03 targeting idiopathic pulmonary fibrosis (IPF) — a progressive, fatal lung disease with median survival of 2–4 years and limited therapeutic options. The company originated as Lung Therapeutics in 2013, was acquired by Aileron Therapeutics in October 2023 (transitioning to public listing), and rebranded to Rein Therapeutics in 2025 to reflect its focus on controlling fibrosis.

The core technology centers on a synthetic peptide derived from the Caveolin-1 scaffolding domain (CSD) — a seven-amino-acid sequence that regulates lung repair and cellular movement. LTI-03, the lead asset, employs a dual mechanism of action: anti-fibrotic activity (modulating signaling pathways to inhibit fibroblast activation and tissue scarring) and regenerative activity (protecting alveolar epithelial cells essential for lung function). It is delivered via a dry powder inhaler for direct-to-lung treatment, offering localized delivery with reduced systemic side effects. Two earlier-stage assets round out the pipeline: LTI-01, a proenzyme (zymogen) for loculated pleural effusion that enzymatically breaks down fibrous scar tissue, and LTI-05 for cystic fibrosis.

As a pre-revenue company, Rein Therapeutics has no commercially approved products and generates no operating revenue; its enterprise value is entirely contingent on clinical milestones and pipeline progression. The company funds operations through equity raises, most recently completing a $57.5 million underwritten public offering in May 2026 expected to fund operations into Q1 2028. Its GTM strategy centers on generating clinical data from the Phase 2 RENEW trial (approximately 120 patients across up to 50 sites in five countries) to support FDA and EMA approvals. Upon regulatory approval, the company would distribute through specialty pharmacy and hospital formulary channels.

Rein Therapeutics firmographics

Firmographics
Name
Rein Therapeutics
Legal name
Rein Therapeutics, Inc.
Website
https://reintx.com
Company type
Public
Founded year
2013
Operating status
Operating
Headcount range
11–50 employees
Short description
Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class Caveolin-1-derived peptide therapeutics for orphan pulmonary and fibrosis indications, with lead candidate LTI-03 in Phase 2 for idiopathic pulmonary fibrosis and earlier-stage pipeline assets for pleural effusion and cystic fibrosis.
Ownership category
akta.pro rank

Rein Therapeutics industry classification

Industry
Product category
Pulmonary Fibrosis Therapeutics
NAICS
Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Pulmonary Hypertension & Rare Pulmonary Disease Therapies (HLAIAIAG)
akta.pro secondary industry
Therapeutic Peptides & Protein/Peptide Biologics (HLAAAAAH)

Keywords

  • Pulmonary fibrosis treatments
  • Orphan pulmonary disease
  • Fibrosis drug development
  • Respiratory therapeutics
  • Inhaled peptide therapy

Where Rein Therapeutics is headquartered

Location

Headquarters

HQ city
Austin
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Rein Therapeutics business model

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

Revenue model

  1. Drug Development and Commercialization: Pre-revenue clinical-stage biopharmaceutical company developing first-in-class medicines for orphan pulmonary and fibrosis indications. Revenue will come from product sales upon regulatory approval of LTI-03 (IPF), LTI-01 (LPE), and LTI-05 (Cystic fibrosis).

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Rein Therapeutics product offering

Product offering

Core offering

Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class synthetic peptide drug candidates for orphan pulmonary and fibrosis indications. Its lead product, LTI-03, is a synthetic peptide derived from Caveolin-1 delivered via dry powder inhaler for the treatment of idiopathic pulmonary fibrosis (IPF), combining anti-fibrotic and regenerative mechanisms of action. The pipeline also includes LTI-01 for loculated pleural effusion and LTI-05 for cystic fibrosis.

Product overview

Rein Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of first-in-class multi-pathway treatments for orphan pulmonary and fibrosis indications. The portfolio consists of three main products: LTI-03 (lead product, Phase 2 for idiopathic pulmonary fibrosis via dry powder inhaler), LTI-01 (preclinical/Phase 1 for loculated pleural effusion), and LTI-05 (preclinical for cystic fibrosis). LTI-03 is the primary focus, targeting both anti-fibrotic and regenerative pathways through a novel Caveolin-1 derived peptide mechanism.

Differentiator

Problem solved

Functional benefit

Products and services

  • LTI-03 First-in-class synthetic peptide derived from Caveolin-1 for the treatment of idiopathic pulmonary fibrosis (IPF). Delivered via dry powder inhaler with dual mechanism of action combining anti-fibrotic effects (inhibiting fibroblast activation and tissue scarring) and regenerative effects (protecting epithelial cells essential for lung function). Currently in Phase 2 RENEW clinical trial.
  • LTI-01 Proenzyme (zymogen) treatment candidate for loculated pleural effusion (LPE), positioned as the first therapy specifically developed for non-draining LPE. Breaks down fibrous tissue, clearing scarred areas and promoting fluid drainage. Currently in preclinical/Phase 1 development.
  • LTI-05 Treatment candidate for cystic fibrosis as part of Rein's multi-pathway fibrotic treatments pipeline addressing orphan pulmonary indications. Currently in preclinical development.

Quantifiable outcome

  • LTI-03 was well tolerated and showed biological activity including reductions in fibrosis biomarkers and preservation of lung repair cells in Phase 1 dose-escalation study
  • +2 more outcomes

Companies that use Rein Therapeutics

Customer profile

Segments3 records

Ideal customer profiles2 records

Rein 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

Rein Therapeutics partnerships and signals

Strategic signal

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

Rein Therapeutics competitors and assessment

Company assessment

Direct peers

  • Pliant Therapeutics: Clinical-stage biopharma developing integrin-targeting therapies for IPF (bexotegrast/PLN-74809) and other fibrotic diseases. Closest direct peer — same indication, similar Phase 2/3 stage, comparable size and orphan-pulmonary focus.
  • FibroGen: Developed pamrevlumab (anti-CTGF) for IPF. Direct comparator in IPF fibrosis drug development with similar clinical-stage positioning and biology-driven approach to fibrotic disease.
  • Avalo Therapeutics: Small clinical-stage biopharma with an inflammation/fibrosis pipeline (formerly Cerecor). Comparable in scale and stage to Rein, focused on immunology and rare pulmonary indications.

Broad incumbents

  • United Therapeutics: Commercial-stage respiratory biopharma with Tyvaso DPI approved for PAH and PH-ILD, adjacent to IPF. A potential strategic acquirer or commercial partner given its established inhaled pulmonary franchise.
  • Boehringer Ingelheim: Markets Ofev (nintedanib), one of two FDA-approved IPF therapies. Sets the standard-of-care bar Rein must clear and is a likely strategic acquirer given its deep respiratory/fibrosis commercial footprint.
  • Roche / Genentech: Markets Esbriet (pirfenidone), the other FDA-approved IPF therapy. Like Boehringer, defines the incumbent treatment paradigm and is a credible strategic acquirer for novel fibrosis mechanisms.
  • Galapagos NV: Had an IPF program (ziritaxestat) discontinued in Phase 3, illustrating both the strategic interest and the high failure rate in fibrosis drug development. Mid-cap European biopharma with adjacent inflammation/fibrosis R&D.
  • Bristol-Myers Squibb: Large biopharma that has invested in IPF/fibrosis through pipeline deals and is a potential strategic acquirer for novel inhaled fibrosis therapies. Sets competitive benchmark for late-stage clinical and commercial resources.

Emerging players

  • PureTech Health: Clinical-stage biopharma with fibrosis and inflammation pipeline programs. Comparable in scale and clinical-stage orphan disease focus, with similar platform-based approach to novel mechanisms.
  • Atea Pharmaceuticals: Small-cap clinical-stage biopharma of similar size, employee count, and NASDAQ-listed profile to Rein Therapeutics, providing a useful comparable for valuation, capital structure, and clinical-stage biotech dynamics.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Rein Therapeutics social profiles

Digital presence

Rein Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Rein Therapeutics leadership team

Management profile

Number of profiles

Profiles7 records

Rein Therapeutics funding detail

Funding detail

Funding overview

Funding rounds13 records

Investors17 records

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

Rein Therapeutics M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Rein Therapeutics

What does Rein Therapeutics do?

Rein Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class synthetic peptide drug candidates for orphan pulmonary and fibrosis indications. Its lead product, LTI-03, is a synthetic peptide derived from Caveolin-1 delivered via dry powder inhaler for the treatment of idiopathic pulmonary fibrosis (IPF), combining anti-fibrotic and regenerative mechanisms of action. The pipeline also includes LTI-01 for loculated pleural effusion and LTI-05 for cystic fibrosis.

Is Rein Therapeutics a public or private company?

Rein Therapeutics is a public company. It is classified as public and is currently operating.

When was Rein Therapeutics founded?

Rein Therapeutics was founded in 2013. It employs 11 to 50 people.

Where is Rein Therapeutics based?

Rein Therapeutics is headquartered in Austin, United States, in the North America region.

How does Rein Therapeutics make money?

One revenue line is on record: drug Development and Commercialization.

Who are Rein Therapeutics's main competitors?

Direct peers on record are Pliant Therapeutics, FibroGen and Avalo Therapeutics. Broad incumbents are United Therapeutics, Boehringer Ingelheim, Roche / Genentech, Galapagos NV and Bristol-Myers Squibb. Emerging players are PureTech Health and Atea Pharmaceuticals.

Does Rein Therapeutics have an API?

No public API is recorded for Rein Therapeutics.

What industry is Rein Therapeutics in?

Rein Therapeutics's product category is Pulmonary Fibrosis Therapeutics. Its primary akta.pro industry code is HLAIAIAG, Pulmonary Hypertension & Rare Pulmonary Disease Therapies, with a secondary code of HLAAAAAH, Therapeutic Peptides & Protein/Peptide Biologics. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
Ticker ReportRein Therapeutics Inc. (NASDAQ:RNTX) Receives Average Rating of “Hold” from AnalystsRein Therapeutics shares received an average analyst rating of "Hold" with a 12-month price target of $6.00. The stock opened at $0.80, and the company reported a quarterly loss of $0.10 per share, beating the consensus estimate of -$0.27. Institutional investors own 90.89% of the company's stock.Stock TitanRein Therapeutics to Present LTI-03 Poster at ERS 2026Rein Therapeutics will present a late-breaking poster on its inhaled peptide LTI-03 for idiopathic pulmonary fibrosis at the ERS 2026 Congress in Barcelona on September 8, 2026. The poster data is published in Nature Communications, and the company's RENEW Phase 2 trial is expected to enroll about 120 patients across five countries.AInvestA Conference Notice Is Not the Story. The RENEW Data Is.Rein Therapeutics announced CEO Brian Windsor will present at two conferences on September 11 and 14, but the key event is the interim RENEW Phase 2 data for LTI-03 in idiopathic pulmonary fibrosis, due in the second half of 2026. The trial's primary endpoint is forced vital capacity, and the company's market value is near zero, making the data point a binary bet.YahooRein Therapeutics to Present at Upcoming September Investor ConferencesRein Therapeutics CEO Brian Windsor will present at the Cantor Global Healthcare Conference on September 11 and the H.C. Wainwright conference on September 14, 2026. The company's lead product candidate LTI-03, a synthetic peptide for pulmonary and fibrosis indications, has received Orphan Drug and Fast Track designations in the U.S.AInvestHere's Why You Should Add RNTX Stock to Your Portfolio NowRein Therapeutics lifted the FDA clinical hold on its LTI-03 IPF study, allowing RENEW to resume. The company has surpassed 25% of planned enrollment and expects interim data in Q4 2026. Shares have fallen 32.7% year-to-date, with a Zacks Rank of Buy.Quiver QuantitativeRein Therapeutics Receives FDA Fast Track Designation for LTI-03 in Idiopathic Pulmonary Fibrosis | RNTX Stock NewsThe U.S. Food and Drug Administration (FDA) has granted Fast Track designation to Rein Therapeutics' drug candidate LTI-03 for the treatment of idiopathic pulmonary fibrosis. This designation facilitates expedited development and review for the inhaled peptide therapy, which is currently being evaluated in an ongoing Phase 2 trial enrolling approximately 120 patients across multiple countries.Investing.comRein Therapeutics receives FDA fast track for IPF drug LTI-03 By Investing.comRein Therapeutics announced that the U.S. Food and Drug Administration has granted Fast Track designation to its experimental drug LTI-03 for the treatment of idiopathic pulmonary fibrosis. The company is currently enrolling patients in a Phase 2 trial across five countries and expects to report interim data in the second half of 2026.Stock TitanRein Therapeutics: FDA Fast Track Designation for LTI-03Rein Therapeutics received Fast Track designation from the U.S. FDA for its investigational drug LTI-03, intended to treat idiopathic pulmonary fibrosis. The company is currently enrolling patients in the Phase 2 RENEW trial across five countries and anticipates reporting interim data in the second half of 2026.BioSpaceRein Therapeutics Receives U.S. FDA Fast Track Designation for LTI-03 in Idiopathic Pulmonary FibrosisRein Therapeutics received FDA Fast Track designation for LTI-03 for idiopathic pulmonary fibrosis. The company is actively enrolling patients in the RENEW Phase 2 trial, on track to report interim data in the second half of 2026. LTI-03 has also received Orphan Drug designation.Investing.comH.C. Wainwright reiterates Buy on Rein Therapeutics stock By Investing.comH.C. Wainwright reiterated a Buy rating on Rein Therapeutics with an $8.00 price target, citing the company's strong liquidity and execution on its Phase 2 RENEW clinical trial for idiopathic pulmonary fibrosis. The firm adjusted its price target downward from $10.00 to account for dilution from Rein Therapeutics' recent $57.5 million equity offering, while noting that enrollment has surpassed 25% of planned patients across five countries.