COMPARISON

Calcitonin vs Teriparatide

6 attributes held for at least one of the two. 6 differ. Each value carries the register it came from and the date that register was read.

Answer

Calcitonin is authorised or registered in 8 and Teriparatide in 10 of the 10 registers read. Calcitonin: highest phase Phase 4 (after approval). Teriparatide: highest phase Phase 4 (after approval). 5 registered trials include both.

States no view on which is preferable, safer or more effective. Not medical advice.

CalcitoninTeriparatide
Registered trials
differs
154
clinicaltrials.gov · 2026-10-03
185
clinicaltrials.gov · 2026-10-03
FDA label
differs
FDA-approved: CALCITONIN SALMON
openfda · 2026-10-03T17:23:44.062Z
FDA-approved: teriparatide
openfda · 2026-10-03T17:23:44.062Z
EU authorisation
differs
Withdrawn
ema · 2026-10-03
Authorised
ema · 2026-10-03
EU authorised on
differs
Not checked
no record of "authorisedOn" for calcitonin
2003-06-10
ema · 2026-10-03
EU withdrawn on
differs
2008-11-20
ema · 2026-10-03
2020-11-24
ema · 2026-10-03
ATC code
differs
H05BA01
ema · 2026-10-03
H05AA02
ema · 2026-10-03

SIDE EFFECTS

Most common side effects, each beside its own placebo

Side effectCalcitoninplaceboTeriparatideplacebo
Arthralgia16.5%21.9%9.1%9.2%
Nausea14.8%3.0%6.3%3.8%
Back Pain10.0%10.6%9.5%10.2%
Nasopharyngitis6.8%8.0%14.1%13.4%
Dizziness6.2%3.3%6.8%5.2%
Hot flush16.9%4.3%--
Dyspepsia9.2%4.1%--
Diarrhoea8.7%5.3%--
Influenza7.0%6.9%--
Hypertension6.0%7.7%--
Hypercalciuria--11.3%6.7%
Headache--7.6%6.5%
Upper respiratory tract infection--7.0%5.6%
Pain in extremity--6.0%5.2%
Constipation--5.3%4.5%

Trial register Calcitonin: 2 placebo-controlled trials; Teriparatide: 11. Each peptide is compared with placebo in its own trials, not with the other: a dash means the event is not in that peptide's top list. Calcitonin side effects · Teriparatide side effects

LEGAL STATUS

Approval in each country read

CountryCalcitoninTeriparatideRegister
United StatesFDA-approvedFDA-approvedRegulator FDA
European UnionWithdrawnAuthorisedRegulator EMA
United KingdomAuthorisedAuthorisedRegulator MHRA
CanadaAuthorisedAuthorisedRegulator Health Canada
AustraliaRegisteredRegisteredRegulator TGA
SwitzerlandAuthorisedAuthorisedRegulator Swissmedic
BrazilRegistadoRegistadoRegulator ANVISA
SerbiaNot on the registerAuthorisedRegulator ALIMS
SingaporeRegisteredRegisteredRegulator HSA
TurkeyRuhsatliRuhsatliRegulator TITCK

HEAD TO HEAD

5 registered trials include both

NCT05366621Post-fracture Medication and Mortality
COMPLETED · updated 2023-04-04
NCT00414973A Study for Patients With Osteoporosis
COMPLETED · updated 2009-10-28
NCT00542984Comparison Medications in the Treatment of Postmenopausal Women With Osteoporosis
COMPLETED · updated 2007-10-12
NCT00543023A Study of the Treatment of Postmenopausal Women With Osteoporosis
COMPLETED · updated 2007-10-12
NCT00543218PTH Comparison in Post Menopausal Women
COMPLETED · updated 2007-10-12

Values reproduce public registers on the dates shown. This comparison states no view on which compound is preferable, safer or more effective. Not medical, legal or regulatory advice.

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