Calcitonin
Regulatory activity · MHRAAlso known as CT - Calcitonin, Thyrocalcitonin.
Recent clinical, regulatory, research and industry developments relating to this drug.
Pharmacologic Treatment of Congenital Nephrogenic Diabetes Insipidus
Evaluation of FGF-23 Suppressibility by Calcitonin in Healthy Men - Pilot Study
Drug Safety Update: Calcitonin (Miacalcic): increased risk of cancer with long-term use
Phase II Study of Calcitonin for Tumoral Calcinosis
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Regulatory timeline
The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.
Contains public sector information from the Medicines and Healthcare products Regulatory Agency (MHRA) licensed under the Open Government Licence (OGL v3).
Clinical trials
The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.
Late-stage studies
Phase III+ trials still open or recently active — where late-stage evidence is being generated.
Recent completions
Trials that read out recently, adding to the completed evidence base.
Phase II Study of Calcitonin for Tumoral Calcinosis
Research activity
Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.
Journals, researchers & institutions
- Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research1
- Binkley N1
- Bolognese M1
- Buben CE1
- Gilligan JP1
- Krause DS1
- Miller C1
- Sidorowicz-Bialynicka A1
- Trout R1
- Osteoporosis Clinical Center and Research Program1
- RxNorm (U.S. National Library of Medicine) — drug identity
- Europe PMC — research literature
- ClinicalTrials.gov — clinical trials
- Regulatory event sources are credited in the Regulatory Timeline above.