Results 161 to 170 of about 206,504 (296)
Impact of cryoballoon size adjustability on procedural and clinical outcomes. [PDF]
Kikkoji N +21 more
europepmc +1 more source
Aims Trial run‐in phases are sometimes used to select adherent participants as a strategy to enrich trials, but the methods employed lack clear regulatory guidance and there are concerns about the transparency of reporting. This review aims to characterize the methods used for adherence measurement and public reporting of run‐in studies.
Non Davies +3 more
wiley +1 more source
A soft policy instrument with a hard content? An analysis of national agreements in Swedish multi-level healthcare. [PDF]
Wide J, Feltenius D.
europepmc +1 more source
Aims To evaluate the effects of vepdegestrant, a PROteolysis TArgeting Chimera (PROTAC) oestrogen receptor degrader, on the pharmacokinetics of dabigatran (a P‐glycoprotein [P‐gp] substrate) and rosuvastatin (a breast cancer resistance protein [BCRP] substrate).
Derek Z. Yang +9 more
wiley +1 more source
A qualitative case study of body image in women with breast cancer participating in an exercise program. [PDF]
Mateu P +7 more
europepmc +1 more source
Perceived managerial discretion and firm performance: The moderating role of market competition
Xi-Ping Zhao +2 more
openalex +1 more source
Navigating adverse immunostimulation: A practical guide for clinical researchers
Problem Setting As drug development moves towards more complex products, early clinical development programmes are increasingly hampered by unwanted and/or unexpected activation of the immune system (adverse immune stimulation, AIS). Solution At the Centre for Human Drug Research, we have introduced standardized procedures to make AIS manageable, while
Juliette A. van den Noort +3 more
wiley +1 more source
Agency Discretion and Public Health Service Delivery
Pamela J. Clouser McCann
openalex +2 more sources

