Table III. Pharmacokinetic parameters for rebamipide following oral administration of granules or a tablet at a dose of 100mg in 27 healthy adult male volunteers [mean (SD)] ...

Objective: To investigate the relative bioavailability and bioequivalence, in fasting and fed conditions, of repeated doses of two omeprazole enteric-coated formulations in healthy volunteers.

He also takes a look at the improvements in quality and bioequivalence policies that are currently being addressed and compares them with those policies already in place in developed countries ...

Radyus Research, a global drug development organization from Atlanta, Georgia, is excited to announce a pivotal strategic ...

The honor is underscored by recent news highlighting the strength of the PumasAI team and its technology for the pharmaceutical industry, including: A focus on leading industry workshops to further ...

The FDA will close out April with five target action dates around indications that include pediatric seizures and a ...

The market reached USD 2.16 billion in 2023 and is projected to grow at a CAGR of 7.62% during the forecast period of ...

Pharmacokinetic data also show bioequivalence when the 2 formulations were compared.

"Our in vitro trials with vaginal tract cells showed activity of the medication against six different strains of Candida, full release within four hours, and bioequivalence between the free drug and ...

We are preparing to enter human bioequivalence studies this year and look forward to providing additional updates on this ...

(RTTNews) - The U.S. Food and Drug Administration has approved INGREZZA Sprinkle (valbenazine) capsules, a new oral granules formulation of INGREZZA (valbenazine) capsules prescribed for the treatment ...

These include first-in-human dose escalation, drug-drug interaction, cardiac safety, bioequivalence and bioavailability, metabolism, and excretion studies, as well as pharmacokinetic evaluations in ...