LEXICON PHARMACEUTICALS, INC. (LXRX)
Lexicon Pharmaceuticals, Inc. is a biopharmaceutical company dedicated to the end-to-end process of identifying, advancing, and bringing to market novel therapeutic compounds. Its development pipeline includes orally administered small molecule drug candidates such as Sotagliflozin, which has successfully concluded Phase III clinical studies for treating both heart failure and type 1 diabetes, and LX9211, currently undergoing Phase II clinical development for neuropathic pain. The firm maintains important strategic collaborations and licensing arrangements with pharmaceutical industry leaders, including Bristol-Myers Squibb Company and Genentech, Inc. Established in 1995, Lexicon Pharmaceuticals, Inc. is based in The Woodlands, Texas.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Lexicon Pharmaceuticals, Inc.
- sotagliflozinREADOUTCash runway at this date: 2yr
Trials need funding. See this company's dilution risk and cash position.
- Phase 3Completed
TELESTAR (Telotristat Etiprate for Somatostatin Analogue Not Adequately Controlled Carcinoid Syndrome)
Telotristat etiprate, Placebo-matching telotristat etiprate
Carcinoid Syndrome
NCT01677910Enrollment135StartJan 2013Primary CompletionMar 2016CompletionMar 2016 - Phase 3Completed
Telotristat Etiprate - Expanded Treatment for Patients With Carcinoid Syndrome Symptoms
Telotristat etiprate
Carcinoid Syndrome
NCT02026063Enrollment124StartJan 2014Primary CompletionSep 2018CompletionSep 2018 - Phase 3Completed
Telotristat Etiprate for Carcinoid Syndrome Therapy
Telotristat etiprate, Placebo
Carcinoid Syndrome
NCT02063659Enrollment76StartMar 2014Primary CompletionMar 2016CompletionMar 2016 - Phase 3Completed
Efficacy, Safety, and Tolerability Study of Sotagliflozin as Adjunct Therapy in Adult Patients With Type 1 Diabetes Mellitus Who Have Inadequate Glycemic Control With Insulin Therapy
Placebo, Sotagliflozin
Type 1 Diabetes Mellitus
NCT02384941Enrollment793StartMar 2015Primary CompletionSep 2016CompletionFeb 2017 - Phase 3Completed
Efficacy, Safety, and Tolerability Study of Sotagliflozin as Adjunct Therapy in Adult Patients With Type 1 Diabetes Mellitus Who Have Inadequate Glycemic Control With Insulin Therapy
Sotagliflozin, Sotagliflozin
Type 1 Diabetes Mellitus
NCT02421510Enrollment782StartMay 2015Primary CompletionNov 2016CompletionJun 2017 - Phase 3Completed
A Phase 3 Study to Evaluate the Safety of Sotagliflozin in Patients With Type 1 Diabetes Who Have Inadequate Glycemic Control With Insulin Therapy Alone
Sotagliflozin, Placebo
Type 1 Diabetes Mellitus (T1DM), High Level of Sugar (Glucose) in the Blood
NCT02531035Enrollment1,405StartSep 2015Primary CompletionApr 2017CompletionApr 2017 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Placebo in Patients With Type 2 Diabetes Mellitus Not Currently Treated With Antidiabetic Therapy
Sotagliflozin (SAR439954), Placebo
Type 2 Diabetes Mellitus
NCT02926937Enrollment399StartNov 2016Primary CompletionApr 2019CompletionMay 2019 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Placebo in Patients With Type 2 Diabetes Mellitus on Background of Metformin
Sotagliflozin (SAR439954), Placebo
Type 2 Diabetes Mellitus
NCT02926950Enrollment518StartNov 2016Primary CompletionFeb 2019CompletionMar 2019 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Placebo in Participants With Type 2 Diabetes Mellitus on Background of Sulfonylurea Alone or With Metformin
Sotagliflozin (SAR439954), Placebo
Type 2 Diabetes Mellitus
NCT03066830Enrollment507StartFeb 2017Primary CompletionApr 2019CompletionApr 2019 - Phase 3Completed
A Study to Evaluate Safety and Effects of Sotagliflozin 400 and 200 mg on Glucose Control in Participants With Type 2 Diabetes, Severe Impairment of Kidney Function and Inadequate Blood Sugar Control
Placebo, Sotagliflozin
Type 2 Diabetes Mellitus, Chronic Kidney Disease Stage 4
NCT03242018Enrollment277StartAug 2017Primary CompletionMay 2019CompletionDec 2019 - Phase 3Completed
Safety and Efficacy Study of Sotagliflozin on Glucose Control in Participants With Type 2 Diabetes, Moderate Impairment of Kidney Function, and Inadequate Blood Sugar Control
Placebo, Sotagliflozin
Type 2 Diabetes Mellitus, Chronic Kidney Disease Stage 3
NCT03242252Enrollment787StartAug 2017Primary CompletionMar 2019CompletionOct 2019 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Placebo in Participants With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control While Taking Insulin Alone or With Other Oral Antidiabetic Agents
Sotagliflozin, Insulin glargine (HOE901)
Type 2 Diabetes Mellitus
NCT03285594Enrollment571StartSep 2017Primary CompletionSep 2019CompletionSep 2019 - Phase 3Terminated
Effect of Sotagliflozin on Cardiovascular and Renal Events in Participants With Type 2 Diabetes and Moderate Renal Impairment Who Are at Cardiovascular Risk
Sotagliflozin, Placebo
Heart Failure, Type 2 Diabetes Mellitus +1
NCT03315143Enrollment10,584StartDec 2017Primary CompletionJul 2020CompletionJul 2020 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Glimepiride and Placebo in Participants With Type 2 Diabetes Mellitus That Are Taking Metformin Monotherapy
Sotagliflozin (SAR439954), Glimepiride
Type 2 Diabetes Mellitus
NCT03332771Enrollment954StartDec 2017Primary CompletionAug 2019CompletionSep 2019 - Phase 3Completed
Efficacy and Safety of Sotagliflozin Versus Placebo and Empagliflozin in Participants With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control While Taking a DPP4 Inhibitor Alone or With Metformin
Sotagliflozin, Empagliflozin
Type 2 Diabetes Mellitus
NCT03351478Enrollment770StartNov 2017Primary CompletionMay 2019CompletionMay 2019 - Phase 3Terminated
Efficacy and Bone Safety of Sotagliflozin 400 and 200 mg Versus Placebo in Participants With Type 2 Diabetes Mellitus Who Have Inadequate Glycemic Control
Sotagliflozin, Placebo
Type 2 Diabetes Mellitus
NCT03386344Enrollment376StartFeb 2018Primary CompletionMay 2019CompletionMay 2020 - Phase 3Terminated
Effect of Sotagliflozin on Cardiovascular Events in Participants With Type 2 Diabetes Post Worsening Heart Failure (SOLOIST-WHF Trial)
Sotagliflozin, Placebo
Heart Failure, Type 2 Diabetes Mellitus
NCT03521934Enrollment1,222StartJun 2018Primary CompletionJun 2020CompletionJun 2020 - Phase 3Active, not recruiting
A Study to Evaluate the Efficacy and Safety of Sotagliflozin in Symptomatic Obstructive and Non-obstructive Hypertrophic Cardiomyopathy
Sotagliflozin, Placebo
Obstructive Cardiomyopathy, Hypertrophic, Non-obstructive Hypertrophic Cardiomyopathy
NCT06481891Enrollment500StartSep 2024Primary CompletionJan 2027est.CompletionFeb 2027est. - Phase 2Completed
Study of LX6171 in Elderly Volunteers With Age Associated Memory Impairment
LX6171 High Dose, LX6171 Low Dose
Age-Related Memory Disorders
NCT00691808Enrollment103StartFeb 2008Primary CompletionOct 2008Completion- - Phase 2Completed
Study of LX1031 in Subjects With Non-Constipating Irritable Bowel Syndrome
LX1031 High Dose, LX1031 Low Dose
Irritable Bowel Syndrome
NCT00813098Enrollment155StartDec 2008Primary CompletionJul 2009CompletionAug 2010 - Phase 2Completed
Study of Telotristat Etiprate (LX1606) in Participants With Symptomatic Carcinoid Syndrome Not Managed by Stable-Dose Octreotide Therapy
Telotristat etiprate, Octreotide LAR Depot
Carcinoid Syndrome
NCT00853047Enrollment23StartMar 2009Primary CompletionJun 2014CompletionJun 2014 - Phase 2Completed
Study of LX3305 in Subjects With Active Rheumatoid Arthritis on Stable Methotrexate
LX3305 low dose, LX3305 mid dose
Rheumatoid Arthritis
NCT00903383Enrollment208StartJul 2009Primary CompletionSep 2010Completion- - Phase 2Completed
Study of LX4211 in Subjects With Type 2 Diabetes Mellitus
LX4211 Low Dose, LX4211 High Dose
Type 2 Diabetes Mellitus
NCT00962065Enrollment36StartAug 2009Primary CompletionDec 2009Completion- - Phase 2Completed
Study of Telotristat Etiprate (LX1606) in Participants With Symptomatic Carcinoid Syndrome
Telotristat etiprate
Carcinoid Syndrome
NCT01104415Enrollment15StartJun 2010Primary CompletionFeb 2014CompletionFeb 2014 - Phase 2Completed
Safety and Efficacy of LX4211 With Metformin in Type 2 Diabetes Patients With Inadequate Glycemic Control on Metformin
75 mg LX4211, 200 mg LX4211
Type 2 Diabetes Mellitus
NCT01376557Enrollment299StartJun 2011Primary CompletionMay 2012CompletionMay 2012
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 3 | Completed | Telotristat etiprate, Placebo-matching telotristat etiprate | NCT01677910 |
| Phase 3 | Completed | Telotristat etiprate | NCT02026063 |
| Phase 3 | Completed | Telotristat etiprate, Placebo | NCT02063659 |
| Phase 3 | Completed | Placebo, Sotagliflozin | NCT02384941 |
| Phase 3 | Completed | Sotagliflozin, Sotagliflozin | NCT02421510 |
| Phase 3 | Completed | Sotagliflozin, Placebo | NCT02531035 |
| Phase 3 | Completed | Sotagliflozin (SAR439954), Placebo | NCT02926937 |
| Phase 3 | Completed | Sotagliflozin (SAR439954), Placebo | NCT02926950 |
| Phase 3 | Completed | Sotagliflozin (SAR439954), Placebo | NCT03066830 |
| Phase 3 | Completed | Placebo, Sotagliflozin | NCT03242018 |
| Phase 3 | Completed | Placebo, Sotagliflozin | NCT03242252 |
| Phase 3 | Completed | Sotagliflozin, Insulin glargine (HOE901) | NCT03285594 |
| Phase 3 | Terminated | Sotagliflozin, Placebo | NCT03315143 |
| Phase 3 | Completed | Sotagliflozin (SAR439954), Glimepiride | NCT03332771 |
| Phase 3 | Completed | Sotagliflozin, Empagliflozin | NCT03351478 |
| Phase 3 | Terminated | Sotagliflozin, Placebo | NCT03386344 |
| Phase 3 | Terminated | Sotagliflozin, Placebo | NCT03521934 |
| Phase 3 | Active, not recruiting | Sotagliflozin, Placebo | NCT06481891 |
| Phase 2 | Completed | LX6171 High Dose, LX6171 Low Dose | NCT00691808 |
| Phase 2 | Completed | LX1031 High Dose, LX1031 Low Dose | NCT00813098 |
| Phase 2 | Completed | Telotristat etiprate, Octreotide LAR Depot | NCT00853047 |
| Phase 2 | Completed | LX3305 low dose, LX3305 mid dose | NCT00903383 |
| Phase 2 | Completed | LX4211 Low Dose, LX4211 High Dose | NCT00962065 |
| Phase 2 | Completed | Telotristat etiprate | NCT01104415 |
| Phase 2 | Completed | 75 mg LX4211, 200 mg LX4211 | NCT01376557 |
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