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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

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BioSniper AI · RNTX

Rein Therapeutics, Inc. (RNTX) is a clinical-stage biopharmaceutical company focused on developing its lead product candidate, LTI-03, for which it is conducting a Phase 2 clinical trial (RENEW) and expects to report initial topline data in the fourth quarter of 2026. The company has no approved products or revenue and has historically funded operations through equity offerings, most recently a $57.5 million public offering in May 2026.

Key risk: No revenue or approved products

6.4/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$65.7M

Cash Runway

14.5 mo

Lead Asset

lti-01 (Phase 2)

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 2 clinical trials · 1 catalyst for Rein Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Rein Therapeutics, Inc. (RNTX) is a clinical-stage biopharmaceutical company focused on developing its lead product candidate, LTI-03, for which it is conducting a Phase 2 clinical trial (RENEW) and expects to report initial topline data in the fourth quarter of 2026. The company has no approved products or revenue and has historically funded operations through equity offerings, most recently a $57.5 million public offering in May 2026.

  • Lead product candidate LTI-03 is in a Phase 2 clinical trial (RENEW) with first patient dosed in March 2026 [sec_mda · as of 2026-03-26].
  • Initial interim topline data from the RENEW trial is expected in the fourth quarter of 2026 [sec_mda · as of 2026-03-26].
  • Cash, cash equivalents and investments totaled $43.6 million as of June 30, 2026 [sec_mda · as of 2026-08-14].
  • Net loss was $6.4 million for the three months ended June 30, 2026 [sec_mda · as of 2026-08-14].
  • Accumulated deficit was $413.5 million as of June 30, 2026 [sec_mda · as of 2026-08-14].

What works

  • The company completed a $57.5 million underwritten public offering in May 2026, providing net proceeds of approximately $53.1 million to fund operations [sec_mda · as of 2026-08-14].
  • Cash position improved significantly from $3.2 million at December 31, 2025 to $43.6 million at June 30, 2026, extending the operational runway [sec_mda · as of 2026-08-14].
  • The RENEW Phase 2 trial is enrolling patients across the U.S., UK, Europe and other jurisdictions, indicating a global development strategy [sec_mda · as of 2026-03-26].

What to weigh

  • The company has no approved products and has never generated revenue from product sales [sec_mda · as of 2026-08-14].
  • The company has incurred significant operating losses and negative cash flows from operations since inception, with an accumulated deficit of $413.5 million as of June 30, 2026 [sec_mda · as of 2026-08-14].
  • The company expects to continue incurring significant expenses and operating losses for the foreseeable future as it advances clinical development [sec_mda · as of 2026-08-14].

From the filings

Quoted directly from source documents.

  • LTI-03 Phase 2 trial first patient dosed in March 2026

    In March 2026, we dosed our first patient in the RENEW Phase 2 clinical trial of LTI-03.

    SEC MD&A · March 26, 2026

  • Interim topline data expected Q4 2026

    We expect to report initial interim topline data on some proportion of patients in the fourth quarter of 2026.

    SEC MD&A · March 26, 2026

  • Cash position as of June 30, 2026

    As of June 30, 2026, we had $43.6 million in cash, cash equivalents and investments.

    SEC MD&A · August 14, 2026

  • Accumulated deficit as of June 30, 2026

    As of June 30, 2026, we had an accumulated deficit of $413.5 million.

    SEC MD&A · August 14, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · lti-03 — Phase 2 Readout: lti-03Initial interim topline data from the RENEW Phase 2 trial of LTI-03 is expected by the end of 2026, which will provide early efficacy and safety signals.
Risks & what to watch (3)

Key risks

  • No revenue or approved productsCompany has never generated product revenue and has no approved products, relying entirely on external financing [sec_mda · as of 2026-08-14].
  • Clinical development uncertaintyLTI-03 is in Phase 2; failure to demonstrate efficacy or safety could halt development and impair value [sec_mda · as of 2026-03-26].
  • Significant accumulated deficitAccumulated deficit of $413.5 million as of June 30, 2026 reflects years of losses with no near-term revenue expected [sec_mda · as of 2026-08-14].

What to watch

  • Initial interim topline data from the RENEW Phase 2 trial of LTI-03 expected in Q4 2026 [sec_mda · as of 2026-03-26].
  • Cash burn rate and whether additional financing will be needed after the May 2026 offering proceeds are consumed [sec_mda · as of 2026-08-14].
  • Enrollment progress and any updates on the RENEW trial across U.S., UK, Europe and other jurisdictions [sec_mda · as of 2026-03-26].

Sources: SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway4.0

14.5 months

Financial Health9.7

D/E 0.20 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst Momentum3.0

1 upcoming, next in ~123d

Insider Signal10.0

5 buys · 0 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

43

Total value held

$9.4M

Showing top 10 of 43 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
-

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, Inc. (RNTX) is a clinical-stage biopharmaceutical company focused on developing its lead product candidate, LTI-03, for which it is conducting a Phase 2 clinical trial (RENEW) and expects to report initial topline data in the fourth quarter of 2026. The company has no approved products or revenue and has historically funded operations through equity offerings, most recently a $57.5 million public offering in May 2026.

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).

What is Rein Therapeutics, Inc.'s next catalyst?

Rein Therapeutics, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: lti-03" — expected December 31, 2026.

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.

925 companies232,681 SEC filings21,419 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.