Drug

Dobutamine

As of the edition of 20 October 2026, Dobutamine is a small molecule: marketed, first approved in 1982 (US); acts on ADRB1 and ADRB2; no US protection is listed.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2021
Kind
Small molecule
Brand name
Dobutrex
First approved
1 January 1982 (US)
Approvals on record
14 in 3 regions
Holder of the most recent approval
SUN PHARMACEUTICAL INDUSTRIES EUROPE (PAYS BAS); 5 holders in all
Registered trials
45, 4 stopped early
Disease areas
Heart and blood vessels; Infections; Inherited and neonatal; Lungs and airways; Pregnancy and women's health; Urinary and reproductive

US protection

No US protection is listed.

The FDA registers list no drug-substance patent or exclusivity that counts for this drug.

This is the US only.

Companies that need a new molecule because of this drug

6 company-target rows on route B because of this drug.

Companies on route B for this drug

In the product

6 company-target rows are on route B because of Dobutamine.

Targets

GeneProteinUniProt
ADRB2Beta-2 adrenergic receptorP07550
ADRB1Beta-1 adrenergic receptorP08588

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated181310
Phase 14101
Phase 211333
Phase 35300
Phase 47300
All trials45

Who has held its approvals

CompanyRoleYears
AbbottLater holder and Lead sponsor of trials1993 to now
Baxter HealthcareLater holder1993 to now
PfizerAcquired holder2005 to now
Eli LillyApplicant