amylin analogue

Pramlintide

US: FDA-approvedEU: Not on the registerUK: Not on the registerCA: Not on the registerAU: Status unknownCH: Not on the registerBR: Not on the registerRS: Not on the registerSG: Not on the registerTR: Not on the register

Answer

Pramlintide is authorised or registered in the US: 1 of the 10 registers read. Highest trial phase: Phase 3 (1 phase 3 trial, 0 with posted results). It has 65 registered trials, 5 of them running. Brand names on the FDA label register: Symlinpen.

RegulatorTrial register10 regulators' registers, read 2026-08-31 to 2026-10-03 · ClinicalTrials.gov and EU CTIS, read 2026-10-03

Not medical, legal or regulatory advice.

Registered trials65Trial register ClinicalTrials.gov and EU CTIS
Running now5Trial register recruiting, active or enrolling
Results posted14Trial register with results on the register
Stopped early13.8%Trial register all peptides: 10%

65 trials by status

Trial register
Running 5Completed 44Stopped early 9Status unknown 6Other or not stated 1

ClinicalTrials.gov and EU CTIS · read 2026-10-03 · 14 trials have posted results

Trials first submitted per year

Trial register

ClinicalTrials.gov first-submitted date, last 10 years · read 2026-10-03. 2026 is not complete. 41 trials carry no first-submitted date (EU CTIS publishes none, or the year is outside this range).

Status by jurisdiction

World map
Authorised or registeredNot on the register, or withdrawnNot read yet, or status unknown
WhereStatusRegisterRead
United StatesFDA-approvedFDA, openfda2026-10-03
European UnionNot on the registerEMA, ema2026-08-31
United KingdomNot on the registerMHRA, uk-mhra2026-09-03
CanadaNot on the registerHealth Canada, ca-dpd2026-09-03
AustraliaStatus unknownTGA, au-artgnot read
SwitzerlandNot on the registerSwissmedic, ch-swissmedic2026-09-03
BrazilNot on the registerANVISA, br-anvisa2026-09-03
SerbiaNot on the registerALIMS, rs-alims2026-09-03
SingaporeNot on the registerHSA, sg-hsa2026-09-03
TurkeyNot on the registerTITCK, tr-titck2026-09-03

An EU decision applies in the 30 territories the EU register covers: its member states, and Iceland, Liechtenstein and Norway. A dashed tile has no register read for this peptide.

Side effects

Trial register
5 placebo-controlled trials · 787 people on Pramlintide · grey is placebo
nausea28.5% 4.7%
injection site pruritus14.7% 0.7%
injection site erythema14.5% 0.9%
Upper respiratory tract infection12.1% 10.4%
injection site bruising11.2% 12.3%
ClinicalTrials.gov posted results · read 2026-10-03All side effects

CHANGE ALERTS

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One email when the status of Pramlintide changes on the register. You confirm your address first.

REGISTERED TRIALS

Newest 10 of 65 trials

All 65 trials
NCT07679516
Postprandial Regulation of Bone Perfusion in Healthy Individuals
not yet recruiting participants · register updated 2026-07-09
NCT06422325
Two Way Crossover Closed Loop Study Insulin vs Insulin and Pramlintide
completed · register updated 2026-06-09
NCT03560960
Multi-Center Development of a Novel Diagnostic Test for Alzheimer's Disease
running, but no longer enrolling · register updated 2026-05-28
NCT06619015
Tailoring Obesity Treatment Trial
withdrawn before enrolling anyone · register updated 2026-04-17
NCT07506369
Pancreatic Polypeptide as a Modulator of Amylin- Induced Satiety in Healthy Humans
currently recruiting participants · register updated 2026-04-01
NCT07340775
Hypersensitivity to Amylin in Post-Traumatic Headache
not yet recruiting participants · register updated 2026-01-14
NCT07340788
Amylin-Induced Migraine Attacks Without Aura
not yet recruiting participants · register updated 2026-01-14
2024-510802-10-00
The impact of pramlintide on top of semaglutide in obese people with prediabetes
no status recorded · register updated 2024-12-03
NCT06046417
A Fully Automated Lyumjev and Pramlintide Delivery System for Adults With Type 1 Diabetes
last verified some time ago; the register no longer confirms its status · register updated 2024-04-18
NCT04074317
Phase 2, Randomized, Open-Label, Crossover, PD/PK Study of a Novel Pram-Insulin Co-Formulation in Adults With T1D
completed · register updated 2024-03-27

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