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NCT03776058

Safety, Tolerability, and Clinical Effects of Twice-daily Doses of Cinacalcet (AMG 073) in Adults With Primary Hyperparathyroidism (HPT)

Completed Phase 2 Last updated 14 December 2018
What this trial tests

Phase 2 trial testing Cinacalcet in Primary Hyperparathyroidism in 10 participants. Completed in 26 December 2000.

Timeline
15 June 2000
Primary endpoint
26 December 2000
26 December 2000

Quick facts

Lead sponsorAmgen
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment10
Start date15 June 2000
Primary completion26 December 2000
Estimated completion26 December 2000

Drugs / interventions tested

Conditions studied

Sponsor

Amgen — full company profile →

Who can join

18 and older, any sex, with Primary Hyperparathyroidism. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objectives were to assess the safety and tolerability of twice daily (BID) doses of 65 mg cinacalcet administered orally to adults with primary HPT.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Cinacalcet

Trials testing the same drug.

Other recruiting trials for Primary Hyperparathyroidism

Currently open trials in the same condition.

Other Amgen trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03776058.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing