ClinicalTrials.gg
RecruitingNCT07583563Updated Oct 27, 2026

An Observational Study of Octreotide Subcutaneous Depot in Patients With Acromegaly

An observational study in Acromegaly, sponsored by Camurus AB. Recruiting at 7 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Camurus AB · Observational

From the registry’s dates

  • Started Jun 2026; still recruiting 5 months later.
Updated Oct 27, 2026Site recruiting status changed1 site addedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to collect long-term (up to two years) safety and effectiveness of octreotide subcutaneous depot in patients with acromegaly in the real-world setting.

02

Conditions studied

  • Acromegaly

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Keywords

  • Octreotide subcutaneous depot
  • Acromegaly
  • Observational
  • Real-world
  • Safety
  • Tolerability
03

In context

Acromegaly

202 studies on the registry are indexed under Acromegaly; 19 are open to participants now.

This study's planned enrollment of 200 is above the median of 100 across 81 observational studies indexed under Acromegaly.

Browse Acromegaly studies →

Lead sponsor

Camurus AB is the lead sponsor of 9 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study will enroll patients with acromegaly who are considered for treatment with octreotide subcutaneous depot and patients with acromegaly who have already initiated octreotide subcutaneous depot treatment. The study will be conducted in Germany, the UK, and the US.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Have started or will be starting treatment with octreotide SC depot for acromegaly

Exclusion criteria

Exclusion Criteria:

  • Have started or will be starting treatment with octreotide SC depot for other conditions not related to acromegaly
  • Currently taking part in an interventional clinical trial or is still within a 30-day from the end of taking part in an interventional clinical trial.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Washout period

A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)
Patient registry
No

Interventions

  • DrugOctreotide subcutaneous depot

    Commercially available octreotide subcutaneous depot treatment administered by participants for a maximum duration up to 2 years in the study

06

What researchers measure

Primary outcomes

  1. Incidence of octreotide SC depot-related AEs and SAEs during 2 years of treatment. Focus is on related AESIs and Other Safety Information.

    Time frame: From enrollment to the end of treatment at 2 years

Secondary outcomes

  1. Change in absolute IGF-1 levels and relative IGF-1 (IGF-1/ULN) over time.

    Time frame: From enrollment to the end of treatment at 2 years

  2. Change in proportion of participants with IGF-1 ≤1×ULN over time.

    Time frame: From enrollment to the end of treatment at 2 years

  3. Change in GH levels over time.

    Time frame: From enrollment to the end of treatment at 2 years

  4. Change in proportion of participants with GH levels <1.0 μg/L over time.

    Time frame: From enrollment to the end of treatment at 2 years

  5. Changes in symptoms of acromegaly over time, as measured by the Acromegaly Index of Severity (AIS) scale.

    The clinician-reported AIS Overall Score ranges from 0 to 18, where a higher score indicates more severe symptoms.

    Time frame: From enrollment to the end of treatment at 2 years

  6. Changes in QoL over time, as measured by the Acromegaly Quality of Life Questionnaire (AcroQoL).

    The AcroQoL domain scores range from 0 to 100, where a higher score indicates better quality of life.

    Time frame: From enrollment to the end of treatment at 2 years

  7. Changes in QoL over time, as measured by the Treatment Satisfaction Questionnaire for Medication (TSQM).

    The TSQM domain scores range from 0 to 100, where a higher score indicates greater treatment satisfaction.

    Time frame: From enrollment to the end of treatment at 2 years

  8. Changes in QoL over time, as measured by the Assessment of Acromegaly Symptoms (AAS) questionnaire.

    The patient-reported AAS total score ranges from 0 to 48, where a higher score indicates more severe symptoms.

    Time frame: From enrollment to the end of treatment at 2 years

  9. Incidence of octreotide SC depot non-related AEs and incidence of laboratory abnormalities using the CTCAE grading scale.

    Time frame: From enrollment to the end of treatment at 2 years

07

Study locations

4 of 7 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Sites
1 site added. Universitaetsklinikum Aachen is now Recruiting
Show site
  • Universitätsklinikum Münster · Münster, Germany
across 2 updates, Sep 25, 2026 – Oct 27, 2026
Show all 2 updates
  1. Oct 27, 2026
    1 site added
    Show site
    • Universitätsklinikum Münster · Münster, Germany
    + 1 other change: verification date
  2. Sep 25, 2026
    Universitaetsklinikum Aachen is now Recruiting
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07583563
Lead sponsor
Camurus AB
Responsible party
Sponsor
First posted
May 13, 2026
Start date
Jun 5, 2026
Primary completion
Jun 2029 (estimated)
Completion
Jun 2029 (estimated)
Last update
Oct 27, 2026

Study contacts

Camurus AB
Contact
medicalinfo@camurus.com
+46 46 286 57 30
View the source record on ClinicalTrials.gov ↗

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