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Kusajili – Clinical trials directory
Result
of your search per sponsor: Lexicon Pharmaceuticals, Inc
Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
Efficacy and safety of adding LX4211 (an investigational oral compound) for patients with Type 1 Diabetes Mellitus (T1D) who have inadequate control of their blood glucose (sugar) levels on insulin alone
The primary objective of this study is to demonstrate superiority of either LX4211 400 mg or 200 mg versus placebo on glycosylated hemoglobin A1C (A1C) reduction at Week 24 when used as an adjunct in ...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Phase 2, Multi-center, Randomized, Double-blind, Placebo-controlled, Multiple-dose Study to Determine the Safety and Efficacy of Daily Orally Administered LX3305 in Subjects with Active Rheumatoid Arthritis (RA) on Stable Methotrexate (MTX) Therapy
The primary objectives of this study are: • To evaluate the safety and tolerability of three dose levels of LX3305 over 12 weeks in subjects with active RA who are also receiving stable doses of MTX; ...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A study to examine the advantage of Sotagliflozin in addition to Insulin therapy in patients with Type 1 Diabetes Studie zkoumající výhody sotagliflozinu jako doplňku inzulinové léčby pacientů s diabetem I. typu
To demonstrate the superiority of sotagliflozin 400 mg versus placebo in the proportion of patients with glycosylated A1C <7.0% at Week 24 and no episode of severe hypoglycemia and no episode of diabe...
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Multicenter, Long-term Extension Study to Further Evaluate the Safety and Tolerability of Telotristat Etiprate (LX1606)
The primary objective of this study is to evaluate the long-term safety and tolerability of orally administered telotristat etiprate
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Phase 2, Open-Label, Multi-Center, Serial Ascending-Dose, Dose Finding Study to Evaluate the Safety and Tolerability of LX1606 in Subjects with Symptomatic Carcinoid Syndrome
The primary objective of this study is to evaluate the safety and tolerability of orally administered LX1606 in subjects with symptomatic carcinoid syndrome.
Country
None
organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Phase 3, Randomized, Placebo-controlled, Multicenter, Double-blind Study to Evaluate the Safety and Efficacy of Telotristat Etiprate (LX1606) in Patients with Carcinoid Syndrome Estudio en fase 3, aleatorizado, multicéntrico, doble ciego y controlado con placebo para evaluar la seguridad y la eficacia de etiprato de telotristat (LX1606) en pacientes con síndrome carcinoide
To evaluate the effect of telotristat etiprate versus placebo over the double-blind portion of the study on the incidence of treatment-emergent adverse events (TEAEs) Evaluar el efecto del etipr...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Research Study of the Efficacy and Safety of Telotristat Etiprate for Carcinoid Syndrome Patients, Who Do Not Respond to Somatostatin Analogue Therapy Studio Clinico per valutare l'efficacia e la sicureza di telotristat etiprato per i pazienti con sindrome da carcinoide (SC) che non rispondono alla terapia con analoghi della somatostatina
The primary objective of the study is to confirm that at least 1 or more doses of telotristat etiprate compared to placebo is effective in reducing the change from baseline in the number of daily bo...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Lexicon Pharmaceuticals, Inc
Update Il y a 5 ans
A Pilot Study to Evaluate Safety and Efficacy of LX1606 in Subjects With Acute, Mild to Moderate Ulcerative Colitis
The primary objective of this study is to evaluate the safety and tolerability of orally administered LX1606 after 8 weeks in a cohort of subjects with acute, mild to moderate ulcerative colitis.
Country
None
organs
None
Specialty
None
Closed trial
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