RNTX
NASDAQRein Therapeutics Inc.
News25/Ratings2
News · 26 weeks13-100%
2025-10-262026-04-19
Mix490d
- SEC Filings3(75%)
- Other1(25%)
Latest news
25 items- SECSEC Form 10-K filed by Rein Therapeutics Inc.10-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Doses First Patient in Phase 2 Trial of LTI-03 for Idiopathic Pulmonary FibrosisAUSTIN, Texas, March 03, 2026 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, announced that it has dosed the first patient in its Phase 2 clinical trial evaluating LTI-03 for idiopathic pulmonary fibrosis (IPF), a progressive and fatal lung disease with limited treatment options. This milestone follows the FDA's recent clearance to resume the Phase 2 program and reflects Rein's successful efforts to address the Agency's requests and advance the trial. The Phase 2 study is a randomized, double-blind, place
- SECRein Therapeutics Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECSEC Form 8-K filed by Rein Therapeutics Inc.8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Receives Orphan Drug Designation from European Medicines Agency for Lead Drug Candidate in Idiopathic Pulmonary FibrosisAUSTIN, Texas, Jan. 20, 2026 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, announced that it has received orphan drug designation from the European Medicines Agency (EMA) for LTI-03, its lead drug candidate aimed at preserving lung function in patients with idiopathic pulmonary fibrosis (IPF). The designation follows a positive opinion from the EMA's Committee for Orphan Medicinal Products (COMP) and subsequent adoption by the European Commission, recognizing both the seriousness of IPF and the need for
- SECRein Therapeutics Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECSEC Form 8-K filed by Rein Therapeutics Inc.8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- INSIDERLarge owner Voss Capital, Lp bought $127,593 worth of shares (104,183 units at $1.22) (SEC Form 4)4 - Rein Therapeutics, Inc. (0001420565) (Issuer)
- SECSEC Form 10-Q filed by Rein Therapeutics Inc.10-Q - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Announces New Scientific Publication Demonstrating LTI-03 May Reduce Lung Scarring and Protect Cells Needed for Lung Repair in IPFAUSTIN, Texas, Nov. 06, 2025 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, announced that a new preprint has been posted to medRxiv describing clinical and translational findings from an inhaled, dose-escalation study of Rein's lead drug candidate, LTI-03, in idiopathic pulmonary fibrosis (IPF). The preprint, titled "Inhaled LTI-03 for Idiopathic Pulmonary Fibrosis: A Randomized Dose Escalation Study," was authored by an international team of investigators, including Philip L. Molyneaux, MD, Nikhil A. Hi
- SECRein Therapeutics Inc. filed SEC Form 8-K: Other Events8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Receives FDA Clearance to Resume U.S. Phase 2 Trial of LTI-03 in Idiopathic Pulmonary FibrosisFDA lifts clinical hold following review of Company's Complete Response submission.Company expects to restart U.S. enrollment in late 2025 or early 2026 across 20 clinical sites.Early data suggests that LTI-03 may not only slow fibrosis but also promote lung healing. AUSTIN, Texas, Nov. 03, 2025 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, today announced that the U.S. Food and Drug Administration (FDA) has lifted the full clinical hold on the Company's Phase 2 "RENEW" trial evaluating LTI-03 in patient
- INSIDERLarge owner Voss Capital, Lp bought $423,466 worth of shares (306,050 units at $1.38) (SEC Form 4)4 - Rein Therapeutics, Inc. (0001420565) (Issuer)
- SECRein Therapeutics Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECSEC Form 8-K filed by Rein Therapeutics Inc.8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Receives European Regulatory Approval to Initiate Phase 2 Trial of LTI-03 in Idiopathic Pulmonary FibrosisEMA approval covers study sites in Germany and Poland as part of the Company's global Phase 2 RENEW trialTrial will evaluate LTI-03, a first-in-class therapy designed to both reduce lung scarring and promote repair AUSTIN, Texas, Oct. 09, 2025 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, today announced that it has received authorization from the European Medicines Agency (EMA) to initiate the Company's Phase 2 "RENEW" clinical trial of its lead candidate, LTI-03, for the treatment of idiopathic pulmona
- INSIDERNew insider Voss Capital, Lp claimed ownership of 1,016,208 shares (SEC Form 3)3 - Rein Therapeutics, Inc. (0001420565) (Issuer)
- ANALYSTH.C. Wainwright initiated coverage on Rein Therapeutics with a new price targetH.C. Wainwright initiated coverage of Rein Therapeutics with a rating of Buy and set a new price target of $10.00
- SECSEC Form 8-K filed by Rein Therapeutics Inc.8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Announces Publication of New Translational Data in iScience on Company's Novel Therapy for Idiopathic Pulmonary FibrosisAUSTIN, Texas, Sept. 17, 2025 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, today announced the publication of novel data on its lead drug candidate, LTI-03, in iScience, a peer-reviewed, open-access journal published by Cell Press. The paper, titled "LTI-03 peptide demonstrates anti-fibrotic activity in ex vivo lung slices from IPF patients," reports how LTI-03 was tested directly on lung tissue donated by patients with idiopathic pulmonary fibrosis (IPF) who underwent lung transplant. In this model, LT
- SECRein Therapeutics Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECSEC Form EFFECT filed by Rein Therapeutics Inc.EFFECT - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECSEC Form S-1 filed by Rein Therapeutics Inc.S-1 - Rein Therapeutics, Inc. (0001420565) (Filer)
- SECRein Therapeutics Inc. filed SEC Form 8-K: Other Events8-K - Rein Therapeutics, Inc. (0001420565) (Filer)
- PRRein Therapeutics Wins U.K. Approval to Launch Phase 2 Clinical Trial of LTI-03 in Idiopathic Pulmonary FibrosisAUSTIN, Aug. 19, 2025 (GLOBE NEWSWIRE) -- Rein Therapeutics ("Rein") (NASDAQ:RNTX), a biopharmaceutical company advancing a novel pipeline of first-in-class medicines to address significant unmet medical needs in orphan pulmonary and fibrosis indications, today announced that the UK Medicines and Healthcare products Regulatory Agency (MHRA) has authorized the Company to initiate its Phase 2 "RENEW" clinical trial of LTI-03, the Company's lead drug candidate for idiopathic pulmonary fibrosis (IPF). IPF is a serious, progressive lung disease that affects hundreds of thousands of people worldwide. It scars the lungs, leaving patients short of breath and with limited treatment options. Median