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RNTXNasdaq

Rein Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 2·Austin, TX, United States·CEO: Dr. James Brian Windsor Ph.D.
Rare DiseaseRespiratory

RNTX evidence brief

What we can confirm

BioSniper Score:
7.9 / 10
Market Cap:
$67.7M
Lead Asset:
lti-01 (Phase 2)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $67.7M · Lead Asset: lti-01 (Phase 2)
BioSniper AIPage evidence connected

Prepared research question

What matters most for RNTX—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · RNTX

Rein Therapeutics (RNTX) is a clinical-stage biopharmaceutical company developing novel therapies for orphan pulmonary and fibrosis indications, with its lead candidate LTI-03 in a global Phase 2 trial for idiopathic pulmonary fibrosis (IPF).

Key risk: Cash runway limited

7.9/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$67.7M

Cash Runway

—

Lead Asset

lti-01 (Phase 2)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 2 clinical trials for Rein Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Rein Therapeutics (RNTX) is a clinical-stage biopharmaceutical company developing novel therapies for orphan pulmonary and fibrosis indications, with its lead candidate LTI-03 in a global Phase 2 trial for idiopathic pulmonary fibrosis (IPF).

  • Lead candidate LTI-03 is a peptide in a Phase 2 RENEW trial for IPF; the company surpassed 25% enrollment and expects interim data in the second half of 2026 [news · 2026-08-14].
  • Cash & equivalents were $8.5M as of 2026-06-30, with zero revenue and a net loss of $6.4M for the quarter [sec].
  • Completed an oversubscribed $57.5 million public offering in 2026 [news · 2026-08-14].
  • Development of LTI-01 and preclinical candidates has been suspended indefinitely due to capital limitations [sec_mda · as of 2026-03-26].
  • The company has never generated revenue from product sales or an operating profit [sec_mda · as of 2026-03-26].

What works

  • LTI-03 has demonstrated the ability to protect healthy lung epithelial cells and reduce pro-fibrotic signaling in a Phase 1b trial [sec_mda · as of 2026-08-14].
  • The Phase 2 RENEW trial is enrolling globally across five countries, with initial topline data expected in 2H 2026 [news · 2026-07-21].
  • The company successfully raised $57.5 million in an oversubscribed public offering, supported by healthcare-focused investors [news · 2026-08-14].

What to weigh

  • The company has no approved products and has never generated revenue from product sales [sec_mda · as of 2026-03-26].
  • Cash reserves are limited ($8.5M as of 2026-06-30) relative to ongoing clinical trial costs [sec].
  • Development of LTI-01 and all preclinical candidates has been suspended indefinitely due to capital constraints [sec_mda · as of 2026-03-26].
  • The company has incurred significant operating losses and negative cash flows from operations since inception [sec_mda · as of 2025-08-14].

From the filings

Quoted directly from source documents.

  • LTI-03 is the lead product candidate in clinical development for IPF.

    “We currently have one lead product candidate in clinical development, LTI-03.”

    SEC MD&A · August 14, 2026

  • The Phase 2 RENEW trial surpassed 25% enrollment and interim data is expected in 2H 2026.

    “Surpassed 25% enrollment milestone in the Global Phase 2 RENEW trial evaluating LTI-03 in idiopathic pulmonary fibrosis (IPF); on track to report interim data in the second half of 2026”

    News · August 14, 2026

  • LTI-01 development has been suspended due to capital limitations.

    “current capital limitations, we have suspended development activities for LTI-01 and our candidates in preclinical development focused on fibrosis indications for an indefinite period”

    SEC MD&A · March 26, 2026

  • The company has never generated revenue from product sales.

    “Since inception, we have not generated any revenue from product sales and have incurred significant operating losses and negative cash flows from operations.”

    SEC MD&A · August 14, 2025

Catalyst timeline

  • 2026-02-02 · Phase 2 RENEW trial start — A Phase 2, randomized, double-blind, placebo-controlled study of LTI-03 in IPF patients began enrollment.
  • 2023-07-06 · Phase 1 start — A Phase 1 dose-escalation study of LTI-03 in treatment-naïve IPF subjects was initiated.
Risks & what to watch (4)›

Key risks

  • Cash runway limited — Cash of $8.5M as of 2026-06-30 may not sustain operations through Phase 2 completion without further financing [sec].
  • Single-asset dependency — All resources are allocated to LTI-03; other pipeline programs are suspended indefinitely [sec_mda · as of 2026-03-26].
  • No revenue or profit history — Company has never generated product revenue or operating profit [sec_mda · as of 2026-03-26].
  • Clinical trial execution risk — Phase 2 RENEW trial is ongoing; failure to meet endpoints would be a major setback [news · 2026-08-14].

What to watch

  • Interim topline data from the Phase 2 RENEW trial expected in the second half of 2026 [news · 2026-08-14].
  • Cash burn rate and potential need for additional financing given $8.5M cash as of 2026-06-30 [sec].
  • Any updates on the resumption of LTI-01 or preclinical programs [sec_mda · as of 2026-03-26].
  • Regulatory developments or partnership announcements that could extend cash runway [sec_mda · as of 2026-08-14].

Sources: Catalysts · News · SEC MD&A · Generated September 26, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.7

D/E 0.20 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal10.0

5 buys · 0 sells (180d)

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

46

Total value held

$14.8M

Showing top 10 of 46 institutional holders of Rein Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 21, 2026
% of float
1.7%
Days to cover
5.4
Shares short
487,162
Daily short volume (Oct 12, 2026)
24.3%

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

RNTX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Rein Therapeutics, Inc.?

Rein Therapeutics (RNTX) is a clinical-stage biopharmaceutical company developing novel therapies for orphan pulmonary and fibrosis indications, with its lead candidate LTI-03 in a global Phase 2 trial for idiopathic pulmonary fibrosis (IPF).

What is Rein Therapeutics, Inc.'s lead drug candidate?

Rein Therapeutics, Inc.'s most advanced tracked candidate is lti-01 (Phase 2) for Loculated pleural effusion (LPE).

Who is the CEO of Rein Therapeutics, Inc.?

Dr. James Brian Windsor Ph.D. is the chief executive officer of Rein Therapeutics, Inc. (RNTX).

Where is Rein Therapeutics, Inc. headquartered?

Rein Therapeutics, Inc. (RNTX) is headquartered in Austin, TX, United States.

What therapeutic areas does Rein Therapeutics, Inc. focus on?

Rein Therapeutics, Inc. develops therapies across Rare Disease, Respiratory.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.