CLINICAL TRIALS PROFILE FOR NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
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All Clinical Trials for naproxen sodium; sumatriptan succinate
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT00329355 ↗ | Menstrual Migraine Treatment With TREXIMET (Formerly Known as TREXIMA) | Completed | GlaxoSmithKline | Phase 3 | 2006-05-01 | This study was designed to determine efficacy of TREXIMET (sumatriptan/naproxen sodium), formerly known as TREXIMA compared to placebo for the treatment of a menstrual migraine. |
| NCT00329459 ↗ | Treximet (Sumatriptan/Naproxen Sodium), Formerly Known as TREXIMA, for Menstrual Migraine in Women With Dysmenorrhea | Completed | GlaxoSmithKline | Phase 3 | 2006-05-01 | This study was designed to determine efficacy of TREXIMA compared to placebo for the treatment of a menstrual migraine. |
| NCT00382993 ↗ | A Study of Combination Product (Sumatriptan Succinate and Naproxen Sodium) in Migraine Subjects Who Report Poor Response or Intolerance to Short Acting Triptans (Study 2 of 2) | Completed | GlaxoSmithKline | Phase 3 | 2006-12-01 | This is a randomized, double-blind, placebo-controlled, crossover, two-attack, out-patient, early-intervention evaluation of subjects who have migraine with or without aura and who discontinued use of short acting triptan(s) within the past year due to non-response or intolerance. Subjects will treat 2 separate migraine attacks during the mild phase of each attack; one attack will be treated with one tablet of the Combination Product (sumatriptan succinate and naproxen sodium) and the other attack with one tablet of placebo (crossover design). [Study 2 of 2] |
| NCT00383162 ↗ | A Study of Combination Product (Sumatriptan Succinate and Naproxen Sodium) in Migraine Subjects Who Report Poor Response or Intolerance to Short Acting Triptans (Study 1 of 2) | Completed | GlaxoSmithKline | Phase 3 | 2006-11-01 | This is a randomized, double-blind, placebo-controlled, crossover, two-attack, out-patient, early-intervention evaluation of subjects who have migraine with or without aura and who discontinued use of short acting triptan(s) within the past year due to non-response or intolerance. Subjects will treat 2 separate migraine attacks during the mild phase of each attack; one attack will be treated with one tablet of the Combination Product (sumatriptan succinate and naproxen sodium) and the other attack with one tablet of placebo (crossover design). [Study 1 of 2] |
| NCT00387881 ↗ | TREXIMET (Formerly Known as TREXIMA) for the Acute Treatment of Probable Migraine (ICHD-II 1.6.1) | Completed | GlaxoSmithKline | Phase 3 | 2006-09-01 | This study was designed to determine the efficacy and tolerability of TREXIMET (formerly known as TREXIMA) compared to placebo for the acute treatment of probable migraine, a sub-type of migraine. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for naproxen sodium; sumatriptan succinate
Condition Name
Clinical Trial Locations for naproxen sodium; sumatriptan succinate
Trials by Country
Clinical Trial Progress for naproxen sodium; sumatriptan succinate
Clinical Trial Phase
Clinical Trial Sponsors for naproxen sodium; sumatriptan succinate
Sponsor Name
| Sponsor Name for naproxen sodium; sumatriptan succinate | |
| Sponsor | Trials |
| GlaxoSmithKline | 9 |
| The Second Hospital of Nanjing Medical University | 1 |
| The Third Xiangya Hospital of Central South University | 1 |
| [disabled in preview] | 2 |
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