Rein Therapeutics, Inc. (RNTX)
Rein Therapeutics Inc. operates as a clinical-stage biopharmaceutical enterprise focused on discovering and bringing to market novel therapeutic solutions for various conditions, notably cancer. The company's leading drug candidate, ALRN-6924, is a distinctive cell-penetrating peptide. This compound works by disrupting the harmful interaction between the p53 suppressor proteins, MDM2 and MDMX, and the vital p53 tumor suppressor. Its goal is to reactivate the natural tumor-suppressing pathways in cancers where the p53 gene is still functional, or "wild-type." The organization was founded on August 6, 2001, by Gregory L. Verdine, Rosana Kapeller, Huw M. Nash, Joseph A. Yanchik III, and Loren David Walensky, and its main corporate offices are situated in Austin, Texas.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Rein Therapeutics Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 2Completed
A Study to Evaluate LTI-01 in Patients With Infected, Non-draining Pleural Effusions
LTI-01, Placebo
Pleural Effusion
NCT04159831Enrollment44StartSep 2020Primary CompletionMar 2022CompletionJul 2022 - Phase 2Recruiting
A Phase 2 Study of LTI-03 in Patients With Idiopathic Pulmonary Fibrosis
LTI-03, Placebo
Idiopathic Pulmonary Fibrosis (IPF)
NCT06968845Enrollment120StartFeb 2026Primary CompletionSep 2027est.CompletionDec 2027est. - Phase 1/2Completed
ALRN-6924 in Patients With Advanced Solid Tumors or Lymphomas
ALRN-6924
Solid Tumor, Lymphoma +1
NCT02264613Enrollment142StartOct 2014Primary CompletionMar 2020CompletionApr 2020 - Phase 1Completed
Phase 1 Safety Study of ALRN-5281 in Healthy Subjects
ALRN-5281 0.015 mg/kg, ALRN-5281 0.05 mg/kg
Growth Hormone Deficiency
NCT01775358Enrollment33StartJan 2013Primary CompletionMay 2013CompletionMay 2013 - Phase 1Completed
Safety Study of ALRN-6924 in Patients With Acute Myeloid Leukemia or Advanced Myelodysplastic Syndrome
ALRN-6924, ALRN-6924 in combination with cytarabine
Acute Myeloid Leukemia, Myelodysplastic Syndromes
NCT02909972Enrollment55StartSep 2016Primary CompletionApr 2019CompletionAug 2019 - Phase 1Terminated
A Study of ALRN-6924 for the Prevention of Chemotherapy-induced Side Effects (Chemoprotection)
ALRN-6924, Carboplatin
Non Small Cell Lung Cancer, Small-cell Lung Cancer
NCT04022876Enrollment35StartSep 2019Primary CompletionJul 2022CompletionAug 2022 - Phase 1Completed
Safety, Tolerability and Pharmacokinetic Study of LTI-03 in Healthy Adult Subjects
Caveolin-1-Scaffolding-Protein-Derived Peptide (LTI-03), Placebo
Idiopathic Pulmonary Fibrosis
NCT04233814Enrollment71StartJan 2020Primary CompletionDec 2021CompletionDec 2021 - Phase 1Terminated
A Study of ALRN-6924 for Protection of Chemotherapy-Induced Side Effects in Patients With TP53-Mutant Breast Cancer
ALRN-6924, TAC (doxorubicin 50 mg/m2; cyclophosphamide 500 mg/m2; docetaxel 75 mg/m2)
Prevention of Chemotherapy-induced Myelosuppression
NCT05622058Enrollment6StartJan 2023Primary CompletionFeb 2023CompletionFeb 2023 - Phase 1Completed
A Study to Evaluate LTI-03 in Newly Diagnosed Idiopathic Pulmonary Fibrosis (IPF) Patients
LTI-03, Placebo
Idiopathic Pulmonary Fibrosis
NCT05954988Enrollment24StartJul 2023Primary CompletionSep 2024CompletionSep 2024
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 2 | Completed | LTI-01, Placebo | NCT04159831 |
| Phase 2 | Recruiting | LTI-03, Placebo | NCT06968845 |
| Phase 1/2 | Completed | ALRN-6924 | NCT02264613 |
| Phase 1 | Completed | ALRN-5281 0.015 mg/kg, ALRN-5281 0.05 mg/kg | NCT01775358 |
| Phase 1 | Completed | ALRN-6924, ALRN-6924 in combination with cytarabine | NCT02909972 |
| Phase 1 | Terminated | ALRN-6924, Carboplatin | NCT04022876 |
| Phase 1 | Completed | Caveolin-1-Scaffolding-Protein-Derived Peptide (LTI-03), Placebo | NCT04233814 |
| Phase 1 | Terminated | ALRN-6924, TAC (doxorubicin 50 mg/m2; cyclophosphamide 500 mg/m2; docetaxel 75 mg/m2) | NCT05622058 |
| Phase 1 | Completed | LTI-03, Placebo | NCT05954988 |