Last reviewed · How we verify

Comparator: loratadine

Organon and Co · Phase 3 active Small molecule

Loratadine is a selective H1-receptor antagonist that blocks histamine-mediated allergic responses without significant central nervous system penetration.

Loratadine is a selective H1-receptor antagonist that blocks histamine-mediated allergic responses without significant central nervous system penetration. Used for Allergic rhinitis (seasonal and perennial), Chronic urticaria.

At a glance

Generic nameComparator: loratadine
SponsorOrganon and Co
Drug classH1-receptor antagonist (second-generation antihistamine)
TargetH1 histamine receptor
ModalitySmall molecule
Therapeutic areaAllergy/Immunology
PhasePhase 3

Mechanism of action

Loratadine competitively binds to peripheral H1 histamine receptors, preventing histamine from triggering allergic symptoms such as itching, sneezing, and urticaria. Its lipophilic structure and large molecular size limit blood-brain barrier penetration, resulting in minimal sedation compared to first-generation antihistamines. It is a non-sedating second-generation antihistamine used for symptomatic relief of allergic conditions.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: