The Effect of Subcutaneous Infusions of 3 Doses of DG3173 on Growth Hormone Levels in Untreated Acromegalics

Brief Title

The Effect of Subcutaneous Infusions of 3 Doses of DG3173 on Growth Hormone Levels in Untreated Acromegalics

Official Title

The Effect of Subcutaneous Infusions of 3 Doses of a Novel Somatostatin Analogue, DG3173, on Growth Hormone Levels in Untreated Acromegalics

Brief Summary

      This study is designed to assess the effect of the different continuous s.c. infusion
      treatments on the human growth hormone (hGH) levels in untreated acromegalic patients in
      comparison to a standard dose of octreotide. In addition, the pharmacokinetic profile and the
      safety and tolerability of DG3173 after continuous s.c. infusion will be evaluated.
    

Study Phase

Phase 2

Study Type

Interventional

Primary Outcome

The Number of Patients Who Achieve a Trough Human Growth Hormone (hGH) Concentration of <2.5µg/L During the Last 12 Hours of the 23 Hour Profile Following Each Study Treatment.

Condition

Acromegaly

Intervention

saline

Study Arms / Comparison Groups

 Saline, then DG3173, then octreotide

Description:  Interventions: saline, DG3173 and octreotide. Eligible patients are to receive a constant 23 hour subcutaneous infusion of saline as placebo comparator and will be randomized in an equal ratio to one of three treatment sequences of doses of 920, 2760 and 5520 µg DG3173 by constant 23 hour subcutaneous infusions in a random sequence followed by three subcutaneous injections of 300 µg octreotide at approximately 8 hour intervals as an active comparator.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Status

Drug

Estimated Enrollment

8

Start Date

November 2013

Completion Date

May 2016

Primary Completion Date

March 2014

Eligibility Criteria

        Inclusion Criteria:

          -  Men, women of non child-bearing potential, or women of child-bearing potential who
             either abstain from sexual intercourse, have a sterile partner or practice two
             medically approved, non-hormonal methods of contraception

          -  Diagnosis of acromegaly of pituitary origin

          -  Have an age-adjusted insulin-like growth factor type 1 (IGF-1) concentration ≥1.2
             times the upper limit of normal range on at least one measurement in the 12 months
             prior to screening (Visit 1) AND a second raised value screening

          -  Have at least one random hGH level of ≥5 μg/L in the 12 months prior to screening AND
             a second raised value at screening

          -  Have given written informed consent

          -  Ability to comply with the requirements of the protocol for the study

        Exclusion Criteria:

          -  Previous specific treatment for acromegaly in the 12 months prior to screening,
             including somatostatin analogues (SSAs); surgery; radiotherapy and pegvisomant

          -  Treatment with dopamine agonists in the 3 months prior to screening

          -  Uncontrolled hypertension

          -  Type I diabetes mellitus, poorly-controlled type II diabetes mellitus (glycosylated
             haemoglobin [HbA1c] ≥7.5%) and patients requiring insulin treatment

          -  Gallstones or gravel that could cause biliary obstruction

          -  Hyperprolactinaemia

          -  Participation in a clinical study within 60 days prior to screening

          -  Receipt of blood, blood products or plasma derivatives 60 days prior to screening

          -  Body mass index (BMI) below 22 or above 37 kg/m2

          -  Pregnancy, lactation or use of any hormonal based contraceptives

          -  Concomitant intake of corticosteroids or levodopa

          -  A history of active alcohol abuse or drug addiction

          -  Positive viral serology screening result for hepatitis B surface antigen, antibodies
             to hepatitis C virus, or human immunodeficiency virus type 1 and 2

          -  Evidence or suspicion of tumour expansion

          -  Clinically significant abnormality in screening ECG in the opinion of the Investigator

          -  Any clinically significant abnormal in screening laboratory safety test (biochemistry,
             haematology and dipstick urinalysis) in the opinion of the Investigator

          -  Any disease which in the Investigator's opinion would exclude the patient from the
             study
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

, , 

NCT ID

NCT02217800

Organization ID

DG3173-II-02

Responsible Party

Sponsor

Study Sponsor

Aspireo Pharmaceuticals Limited

Study Sponsor

, , 

Verification Date

January 2018