Drugs / Sandostatin LAR

Regulatory milestones approvals, filings & regulatory actions · 3 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Label expansions (2) US (FDA) SANDOSTATIN LAR — 2006-05-10 – 2008-03-03 fda.gov ↗
Approved US (FDA) SANDOSTATIN LAR — 1998-11-25 fda.gov ↗

Trials 5

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 45 trials
Phase 4 NCT01618513 Jun 2012 → Jan 2017 acromegaly University of Aarhus Completed No outcome recorded
Phase 4 NCT01278342 Sep 2006 → Nov 2009 acromegaly Novartis Pharmaceuticals Completed No outcome recorded
Phase 4 NCT00076362 Mar 2004 → Jul 2005 obesity disorder Novartis Pharmaceuticals Completed No outcome recorded
Phase 4 NCT00068029 Oct 2003 → May 2006 acromegaly Pfizer Completed No outcome recorded
Phase 4 NCT00068042 Apr 2003 → May 2006 acromegaly Pfizer Completed No outcome recorded
Comparator or background therapy1 trial
Phase 1 NCT05364944 Background May 2022 → Oct 2024 acromegaly, digestive system neuroendocrine neoplasm Debiopharm International SA Terminated No outcome recorded Stop: Enrollment

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as Sandostatin LAR ClinicalTrials.gov intervention name — accepted as the source's own label NCT01278342 ↗
5

NCT05364944 ↗

NCT00068029 ↗

NCT00076362 ↗

NCT00068042 ↗

NCT01618513 ↗

Route Intramuscular “40 mg intramuscular (i.m.) every 28 days for 3 months” NCT01278342 ↗