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Generated: October 20, 2018

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CLINICAL TRIALS PROFILE FOR OVIDREL

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Clinical Trials for OVIDREL

Trial ID Title Status Sponsor Phase Summary
NCT00505752 Investigation of a Long-Acting Follicle Stimulating Hormone in Infertile Women Undergoing Assisted Reproductive Technology (ART) Completed Merck KGaA Phase 2 This is a Phase 2, interventional, prospective, multi-center, randomized, assessor-blind, active-comparator, dose-finding study to evaluate a new investigational long-acting follicle stimulating hormone (FSH) in infertile women who are undergoing an assisted reproductive technology (ART) procedure (In vitro fertilization/Intra cytoplasmic sperm injection [IVF/ICSI]). This study will compare 3 doses of the investigational drug versus a currently marketed drug follitropin alfa (Gonal-f® revised formulation female [RFF] Pen) in regards to the number of fertilized oocytes.
NCT00663416 REGENESIS (CA): A Study of NTx™-265: Human Chorionic Gonadotropin (hCG) and Epoetin Alfa (EPO) in Acute Ischemic Stroke Patients Terminated Stem Cell Therapeutics Corp. Phase 2 Primary objective: To assess the neurological outcome in acute ischemic stroke patients treated with NTx™-265, when compared with patients given a placebo control. Secondary objective: To assess the safety and tolerability of NTx™-265 when given to acute ischemic stroke patients.
NCT00715364 REGENESIS (US): A Phase IIb Prospective, Randomized, Double-blind, Placebo Controlled Study of NTx™-265: Human Chorionic Gonadotropin (hCG) and Epoetin Alfa (EPO) in Acute Ischemic Stroke Patients Withdrawn Stem Cell Therapeutics Corp. Phase 2 To assess the safety and tolerability of NTx™-265 when given to acute ischemic stroke patients. To assess the neurological outcome in acute ischemic stroke patients treated with NTx™-265, when compared with patients given a placebo control.
NCT00747617 Theca Cell Function in Women With Polycystic Ovary Syndrome (PCOS) Completed University of California, San Diego Phase 3 The mechanism for increased androgen production in women with polycystic ovary syndrome (PCOS) is not well understood. Excess androgen production by the ovary is stimulated by increased pituitary luteinizing hormone (LH) secretion in this disorder. The investigators hypothesize that in PCOS women ovarian theca cells, which are responsible for androgen synthesis, are more sensitive to LH stimulation compared to that of theca cells from normal women. To test this hypothesis, the investigators propose to conduct a dose-response study in which androgen responses to multiple doses of human chorionic gonadotgropin (hCG), an LH surrogate, will be assessed in PCOS and normal women.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for OVIDREL

Condition Name

Condition Name for OVIDREL
Intervention Trials
Infertility 12
Stroke 3
Polycystic Ovary Syndrome 2
Ovulation Induction 1
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Condition MeSH

Condition MeSH for OVIDREL
Intervention Trials
Infertility 13
Polycystic Ovary Syndrome 3
Stroke 3
Syndrome 2
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Clinical Trial Locations for OVIDREL

Trials by Country

Trials by Country for OVIDREL
Location Trials
India 12
Canada 10
United States 7
Korea, Republic of 3
China 2
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Trials by US State

Trials by US State for OVIDREL
Location Trials
California 5
Ohio 1
Massachusetts 1
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Clinical Trial Progress for OVIDREL

Clinical Trial Phase

Clinical Trial Phase for OVIDREL
Clinical Trial Phase Trials
Phase 4 2
Phase 3 8
Phase 2 5
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Clinical Trial Status

Clinical Trial Status for OVIDREL
Clinical Trial Phase Trials
Completed 10
Not yet recruiting 4
Terminated 3
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Clinical Trial Sponsors for OVIDREL

Sponsor Name

Sponsor Name for OVIDREL
Sponsor Trials
University of California, San Diego 3
Stem Cell Therapeutics Corp. 3
Merck KGaA 3
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Sponsor Type

Sponsor Type for OVIDREL
Sponsor Trials
Industry 14
Other 13
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Serving hundreds of leading biopharmaceutical companies globally:

Express Scripts
Cantor Fitzgerald
McKinsey
Queensland Health
US Army
Healthtrust
Chubb
Fuji
Daiichi Sankyo

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