The RApid Switch From 1st Generation Somatostatin Analogues to PaSireOtiDe In Acromegaly
Recruiting now
Conditions studied: Acromegaly
In brief
This is an observational, retrospective, national multicenter study aimed to evaluate the impact and efficacy of Time To Switch (TTS) from first-line to second-line medical therapy in Acromegaly.
Key facts
- Study ID
- NCT06597383
- Run by
- IRCCS San Raffaele
- People needed
- 100
- Starts
- 2023-11-24
- Expected to finish
- 2024-11-01
- Last updated by the study team
- 2024-09-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult men and women (age ≥ 18 years) affected by acromegaly, including those of childbearing age
- Patients inadequately controlled with first generation somatostatin analogues (GH ≥1 μg/L and IGF-1 >1.3×ULN)
- Second line medical treatment (Pasireotide; Pegvisomant only; combination Pegvisomant + 1st generation SSA) after use of first-line medical treatment
- At least 12 months of follow up during 2nd line therapy
- Signature of the informed consent to the study
You may not qualify if…
- age ≤18 years
- Pregnant and/or breastfeeding women
- Patients unable to understand and sign the Informed Consent
Where it is running
- Andrea Giustina — Milan, Italy (enrolling)
Full record on ClinicalTrials.gov
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