Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Erin O'Boyle"'
Publikováno v:
The Journal of Community and Supportive Oncology. 13:38-46
BACKGROUND A phase 3 trial in patients with cancer who received chemotherapy has shown that subcutaneous (SC) APF530, a sustained-delivery formulation of granisetron, is noninferior to palonosetron in preventing acute (0-24 hours) and delayed (>24-12
Autor:
Erin O'Boyle, Nashat Y. Gabrail, Harry Raftopoulos, Ralph V. Boccia, Richard J. Gralla, William Cooper
Publikováno v:
Supportive Care in Cancer
Purpose Subcutaneous APF530 provides controlled sustained release of granisetron to prevent acute (0–24 h) and delayed (24–120 h) chemotherapy-induced nausea and vomiting (CINV). This randomized, double-blind phase 3 trial compared APF530 and pal
Publikováno v:
Future oncology (London, England). 11(18)
Background: APF530 is a novel sustained-release formulation of granisetron. In a Phase III trial, APF530 500 mg was noninferior to palonosetron 0.25 mg in preventing acute chemotherapy-induced nausea and vomiting (CINV) after moderately (MEC) or high
Publikováno v:
Cancer Management and Research
Jay W Mason,1 Thomas E Moon,2 Erin O’Boyle,3 Albert Dietz41Department of Medicine, University of Utah, Salt Lake City, UT, 2Tarizona eHealth Services, Inc., San Carlos, CA, 3AP Pharma, Redwood City, CA, 4Spaulding Clinical Research, West Bend, WI,
Autor:
Carrie Smith, Ronald Yanagihara, Marek Spaczyński, William Cooper, Erin O’Boyle, Ralph Boccia, Nash Gabrail
Publikováno v:
Cancer Management and Research
Nashat Gabrail,1 Ronald Yanagihara,2 Marek SpaczyÅski,3 William Cooper,4 Erin O'Boyle,5 Carrie Smith,1 Ralph Boccia6 1Gabrail Cancer Center, Canton, OH, USA; 2St Louise Regional Hospital, Gilroy, CA, USA; 3Department of Gynecology, Obstetrics and
Publikováno v:
Journal of Experimental Pharmacology
Thomas Ottoboni,1 Mark S Gelder,1 Erin O’Boyle2 1Heron Therapeutics, Inc., Redwood City, CA, USA; 2FibroGen, Inc., San Francisco, CA, USA Abstract: Granisetron and other 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists are first-line agents
Publikováno v:
Journal of Clinical Oncology. 32:9648-9648
9648 Background: APF530 provides controlled sustained release of granisetron to prevent acute (0-24 h) and delayed (24-120 h) CINV. In a phase 3 trial in 1395 patients, single doses of subcutaneous...
Publikováno v:
Journal of Clinical Oncology. 32:9645-9645
9645 Background: APF530 provides controlled, sustained release of granisetron for preventing acute (0-24 h) and delayed (24-120 h) CINV. In a phase 3 trial measuring complete response (CR; no emesi...
Publikováno v:
Journal of Clinical Oncology. 31:9626-9626
9626 Background: Patients receiving MEC or HEC were administered subcutaneous (SC) APF530 500 mg, a sustained delivery formulation of granisetron (10 mg). The complete antiemetic response rates (CR; no emetic episodes and no rescue medication) were n
Publikováno v:
Journal of Clinical Oncology. 31:e20539-e20539
e20539 Background: This study evaluated effects of subcutaneous (SC) APF530 (sustained-release granisetron) and intravenous (IV) granisetron on placebo-adjusted change from baseline in QT corrected with the Fridericia method (QTcF) over 48 h (ddQTcF)