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Pharmacokinetics of once weekly dulaglutide in special populations [abstract no

Another renaissance for bile acid gastrointestinal microbiology

Since GLP-1 and GIP are closely related, they thought it might be possible to target both receptors with a single drug

To minimize gastrointestinal side effects, the tirzepatide dose was gradually increased in all SURMOUNT clinical trials, starting at 2.5 mg and escalating by 2.5 mg every 4 weeks until reaching the maintenance dose required

[3] Oral administration is the most pharmacologically unusual option and the one with the strongest theoretical support for gut-specific applications