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Trial · Interventional

TerminatedPhase 2Results postedRegistry data

Pasireotide LAR Therapy of Silent Corticotroph Pituitary Tumors

Short name PASSILCORT

NCTNCT02749227 (opens ClinicalTrials.gov in a new tab)Other idAAAQ6255Other idCSOM230GUS44T

Overview

Status
Terminated
Phase
Phase 2
Enrollment
4 participants (actual)
Sponsor
Columbia University · Other
Design
Allocation not applicable · Open label (no masking)
Countries
1 country

United States

Start
10 Jul 2017
Primary completion
31 Mar 2020
Completion
31 Mar 2020
First posted
22 Apr 2016 (estimated)
Last update posted
27 Apr 2021
Conditions
Pituitary Tumor · ACTH-producing Pituitary Tumour

Timeline

1 trial · 1 stopped early · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
20172018201920202021
  1. Ph 2

    PASSILCORT

    NCT02749227

    10 Jul 2017 to 31 Mar 2020

    Terminated

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

This is a phase II, open-label, 12-month pilot study in 10 patients with silent corticotroph pituitary tumors testing the hypotheses that Pasireotide long-acting release (LAR) treatment of patients with silent corticotroph pituitary tumors and elevated plasma Proopiomelanocortin (POMC) levels will reduce plasma POMC levels and this will be associated with a reduction in pituitary tumor size. Pasireotide LAR 40 mg will be administered monthly. Baseline and monthly visits on therapy will monitor plasma levels of POMC, other pituitary function, safety labs, glucose tolerance, physical examination, and visual fields. Pituitary magnetic resonance imaging (MRI) will be done at baseline, 6 months and 12 months of therapy. The eligible patient population will consist of adult patients with known silent corticotroph pituitary tumors and elevated plasma levels of POMC.

Interventions

  • Pasireotide LARDrug

Arms1

  • Experimental

    Pasireotide LAR Therapy

    Subjects will receive Pasireotide LAR monthly. Safety labs and Pituitary MRI will be performed.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Change in Plasma Proopiomelanocortin (POMC) Levels

    Time frame · Baseline, 12 months

    Registry description

    This is to measure the effect of Pasireotide LAR (long-acting release) treatment.

Secondary outcomes(1)
  1. Change in Pituitary Tumor Volume

    Time frame · Baseline, 12 months

    Registry description

    This is to measure the effect of Pasireotide LAR (long-acting release) treatment.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcome· Baseline, 12 months

Change in Plasma Proopiomelanocortin (POMC) Levels

GroupValue
Pasireotide LAR Therapynot posted
Secondary and other outcome results(1)
Secondary outcome· Baseline, 12 months

Change in Pituitary Tumor Volume

GroupValue
Pasireotide LAR Therapynot posted

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Pasireotide LAR TherapySubjects will receive Pasireotide LAR monthly. Safety labs and Pituitary MRI will be performed. Pasireotide LAR: Pasireotide LAR (SIGNIFOR® LAR) is a somatostatin analog indicated for the treatment of patients with acromegaly who have had an inadequate response to surgery and/or for whom surgery is not an option. It is a long acting release injectable suspension for intramuscular use. The starting dose is Pasireotide LAR 40 mg/month intramuscular (IM), this will be increased to 60 mg/month at 6 months if a fall in POMC levels and/or tumor shrinkage are not attained.0 / 40 / 40 / 4

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 80 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion criteria: Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the study: 1. Adults (males and females) with a diagnosis of a clinically nonfunctioning pituitary tumor of the silent corticotroph tumor type (i.e., positive adrenocorticotropin (ACTH) staining on immunohistochemical staining of the pituitary tumor obtained at surgery) 2. Plasma POMC level \> upper limit of normal 3. Prior pituitary tumor surgery with residual or recurrent pituitary tumor visible on MRI scan that is ≥ 5 mm from the optic chiasm. 4. Surgical resection of the pituitary adenoma must have occurred two or more months prior to enrollment 5. If patients have undergone pituitary radiotherapy they must have completed their course of radiotherapy at least 2 months prior to study screening 6. No prior somatostatin analog therapy 7. No concurrent use of dopamine agonist therapy 8. No active malignancy 9. Stable pituitary hormone supplements (x 2 months) prior to baseline visit 10. Sign and date an informed consent document indicating that the subject has been informed of and agrees to all pertinent aspects of the trial Exclusion criteria: Subjects must not meet any of the following exclusion criteria to be eligible for enrollment into the study: 1. Patients with Cushing's disease (biochemical evidence of hypercortisolism) 2. Patients with compression of the optic chiasm causing any visual field defect that requires surgical intervention 3. Diabetic patients with poor glycemic control as evidenced by HbA1c \>8% 4. Patients who are hypothyroid or adrenally insufficient and not on adequate replacement therapy 5. Patients with symptomatic cholelithiasis and acute or chronic pancreatitis 6. Patients with risk factors for torsade de pointes, i.e., patients with a baseline QTcF (Fridericia's Correction Formula value) \>450 ms in males, and \>460 ms in females 7. Hypokalaemia, hypomagnesaemia, uncontrolled hypothyroidism, family history of long QT syndrome or concomitant medications with known risk of Torsades de pointes (TdP). Drugs with possible risk of TdP should be avoided whenever feasible 8. Patients who have congestive heart failure (NYHA Class III or IV), unstable angina, sustained ventricular tachycardia, clinically significant bradycardia, advanced heart block, history of acute myocardial infarction (MI) less than one year prior to study entry or clinically significant impairment in cardiovascular function 9. Concomitant disease(s) that could prolong the QT interval such as autonomic neuropathy (caused by diabetes or Parkinson's disease), HIV, cirrhosis, uncontrolled hypothyroidism or cardiac failure 10. Patients with liver disease such as cirrhosis, chronic active hepatitis, or chronic persistent hepatitis, or patients with alanine aminotransferase (ALT)/aspartate aminotransferase (AST) \> 2.0 X upper limit of normal (ULN), serum bilirubin \>2.0 X ULN 11. Presence of Hepatitis B surface antigen (HbsAg) or Hepatitis C antibody test (anti-HCV) 12. Patients with serum creatinine \>2.0 X ULN 13. Patients with white blood cell (WBC) count \<3 X 109/L; Hb 90% \< lower limit of normal (LLN); platelet (PLT) count \<100 X 109/L 14. Patients with the presence of active or suspected acute or chronic uncontrolled infection 15. Patients who have undergone major surgery/surgical therapy for any cause within 4 weeks prior screening 16. Patients with abnormal coagulation (PT and/or activated partial thromboplastin time (APTT) elevated by 30% above normal limits) or patients receiving anticoagulants that affect PT (prothrombin time) or APTT (activated partial thromboplastin time) 17. History of syncope or family history of idiopathic sudden death 18. History of immunocompromise, including a positive HIV test result (ELISA and Western blot) 19. Sexually active males unless they use a condom during intercourse while taking drug and for 3 months following last dose of pasireotide and should not father a child in this period. A condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid 20. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive urine pregnancy test 21. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and 3 months following last dose of pasireotide. Highly effective contraception methods include: * Total abstinence when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception * Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment * Male sterilization (at least 6 months prior to screening). For female subjects on the study the vasectomized male partner should be the sole partner for that subject * Combination of any two of the following (a+b or a+c, or b+c): 1. Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate \<1%), for example hormone vaginal ring or transdermal hormone contraception. 2. Placement of an intrauterine device (IUD) or intrauterine system (IUS) 3. Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository * In case of use of oral contraception women should have been stable on the same pill for a minimum of 3 months before taking study treatment. * Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks ago. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential.

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