Search Results for: "Clinic Roundup"
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Clinic Roundup
Under the terms of the agreement, Ariad will receive a $10 million milestone payment from Merck upon treatment of the first patient in the study...The 580-patient study is designed to compare T-DM1, as a single agent, to capecitabine plus lapatinibBioWorld Today | Tuesday, March 3, 2009 -
Clinic Roundup
In addition to EC145, patients in the study also will be treated with a molecular imaging agent, EC20, also developed by Endocyte, which is designed to allow clinicians to identify tumors that overexpress the folate receptorBioWorld Today | Friday, February 20, 2009 -
Clinic Roundup
As a result of the discontinuation, all patients on the study drug will be moved to the standard of careBioWorld Today | Tuesday, February 17, 2009 -
Clinic Roundup
The 10-patient study uses Cytori's Celution 800 System to process and extract the patients' own adipose tissue-derived stem and regenerative cells at the time of surgeryBioWorld Today | Monday, February 2, 2009 -
Clinic Roundup
Those results are now reinforced by those additional findings indicating, in part, that patients in the study quickly returned to their pretreatment level of atrial fibrillation once the treatment endedBioWorld Today | Tuesday, January 13, 2009 -
Clinic Roundup
The 510-patient study met both the primary and secondary endpoints, and Zemiva was well tolerated, with no serious adverse effectsBioWorld Today | Wednesday, December 24, 2008 -
Clinic Roundup
The 469-patient study consisted of an initial four-week, double-blind phase followed by an eight-week open-label phaseBioWorld Today | Monday, December 1, 2008 -
Clinic Roundup
Patients in the study will be followed for 12 months post-treatmentBioWorld Today | Monday, November 24, 2008 -
Clinic Roundup
Anadys expects to enroll approximately 30 patients in the study of ANA598 at doses of 200 mg bid (twice-a-day), 400 mg bid and 800 mg bidBioWorld Today | Thursday, October 30, 2008 -
Clinic Roundup
After 14 days of bevirimat treatment given twice daily at doses of 200 mg or 300 mg, 100 percent of 32 treatment-naive and treatment-experienced patients in Study 204 had bevirimat plasma concentrations well above the previously identified minimum target of 20I 1/4g/mLBioWorld Today | Wednesday, October 29, 2008 -
Clinic Roundup
However, due to the small number of patients in the study, neither of these endpoints were statistically significantBioWorld Today | Tuesday, September 30, 2008 -
Clinic Roundup
Patients in the study are treated once daily with one of three dose levels of VIA-2291, a small-molecule drug that targets inflammation in the blood vessel wall, or placeboBioWorld Today | Thursday, September 25, 2008 -
Clinic Roundup
Napo Pharmaceuticals Inc., of San Francisco, said results from a 100-patient study of crofelemer in severely ill cholera patients in conjunction with an antibiotic and rehydration therapy showed that the drug, dosed at 125 mg every six hours, reduced the amount of stool volume output normalized to a body weight by 32 percent in the first six-hour periodBioWorld Today | Tuesday, September 23, 2008 -
Clinic Roundup
The 80-patient study is evaluating daily TT-223 treatments for 12 weeks with a six-month follow-upBioWorld Today | Monday, September 15, 2008 -
Clinic Roundup
The primary objective of the 14-patient study is to measure tumor responses and duration of response, as well as to describe any evidence of antitumor activityBioWorld Today | Tuesday, September 9, 2008 -
Clinic Roundup
However, a post hoc analysis of patients with a history of aura, which represented 47 percent of all patients in the study, demonstrated statistically significantly sustained pain relief for up to 24 hours without rebound headache, with 22 percent, 48 percent and 68 percent of patients experiencing relief compared to placebo at two hours, four hours and six hours, respectivelyBioWorld Today | Monday, September 8, 2008 -
Clinic Roundup
BMS-099, a 676-patient study, was not powered to detect an improvement in overall survival with the same degree of statistical precision as was the larger 1,125-patient pivotal FLEX Phase III study conducted by Merck KGaA, of Darmstadt, GermanyBioWorld Today | Tuesday, September 2, 2008 -
Clinic Roundup
Data from the 23-patient study showed that, at both dose levels given, PTC124 was associated with statistically significant improvements in CFTR-mediated chloride transport with more than half of the patients entering the normal range during at least one treatment courseBioWorld Today | Friday, August 22, 2008 -
Clinic Roundup
The 80-patient study is designed to test the safety and tolerability of multiple subcutaneous dose schedules of MEDI-545 or placebo in adults with moderate to severe active lupusBioWorld Today | Wednesday, August 13, 2008 -
Clinic Roundup
The three-arm, 180-patient study is designed to determine whether combination therapy is superior to either Vidaza or MGCD0103 aloneBioWorld Today | Thursday, June 26, 2008
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