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Trial · Interventional

CompletedPhase 2Results postedRegistry data

Efficacy of Medical Treatment With SOM230 LAR in Patients With Primary Inoperable Thymoma and/or With Local Recurrent Thymoma to Reduce Tumor Size

Overview

Status
Completed
Phase
Phase 2
Enrollment
16 participants (actual)
Sponsor
Prof. Dr. Berthold Schalke · Other
Design
Allocation not applicable · Open label (no masking)
Countries
1 country

Germany

Start
Mar 2012
Primary completion
Oct 2015
Completion
Oct 2015
First posted
27 Dec 2013 (estimated)
Last update posted
5 Feb 2018
Conditions
Primary Inoperable Thymoma · Local Recurrent Thymoma

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
20122013201420152016
  1. Ph 2

    Efficacy of Medical Treatment With SOM230 LAR in Patients With Primary Inoperable Thymoma and/or With Local Recurrent Thymoma to Reduce Tumor Size

    NCT02021942

    Mar 2012 to Oct 2015

Registry summary

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

This is a monocenter, single-arm, open label phase II trial evaluating the effect of SOM230 LAR in adult patients with inoperable primary thymoma and thymoma metastasis (Masaoka II-IVa). SOM230 LAR in a dosage of 60 mg is administered i.m. once every 4 weeks. The purpose of this trial is a proof of concept.

Interventions

  • SOM230 LARDrug

Arms1

  • Experimental

    SOM230 LAR

    SOM230 LAR in a dosage of 60 mg i.m. once every 4 weeks

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Percent Change in Tumor Volume From Baseline to EOS

    Time frame · at least 6 months

    Registry description

    To evaluate whether SOM230 LAR is effective in patients with inoperable thymoma with respect to shrinkage of tumor volume. Response is defined as the decrease in tumor volume of 20 % at EOS as compared to baseline. Tumor shrinkage is assessed by CT or MRI.

Secondary outcomes(2)
  1. Tumor Resection Status

    Time frame · at least 6 months

    Registry description

    To evaluate the resection status based on the categories R0, R1 and ≥ R2 at EOS using CT or MRI imaging. R0 resection means no residual tumor tissue (best status); R1 indicates microscopic residual tumor tissue and R2 indicates macroscopic residual tumor tissue (worst status).

  2. Assessment of Tumor Operability

    Time frame · at least 6 months

    Registry description

    Assessment if patients reaching operability at the EOS.

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 outcomeMean· at least 6 months

Percent Change in Tumor Volume From Baseline to EOS

GroupValue (percentage of tumor volume)
SOM230 LAR-37.38
Secondary and other outcome results(6)
Secondary outcomeCount of participants· at least 6 months

Tumor Resection Status

GroupValue (Participants)
SOM230 LAR6
Secondary outcomeCount of participants· at least 6 months

Assessment of Tumor Operability

GroupValue (Participants)
SOM230 LAR11
Other pre specified outcomeCount of participants· at least 6 months

Safety: Number of Participants With Adverse Events (AE) and Serious Adverse Events (SAE)

GroupValue (Participants)
SOM230 LAR16
Other pre specified outcomeCount of participants· at least 6 months

Assessment of Myasthenia Gravis (MG) Status by Determining Titin-antibody Status

GroupValue (Participants)
SOM230 LAR8
Other pre specified outcomeCount of participants· at least 6 months

Assessment of Myasthenia Gravis (MG) Status by Measuring ACHR-antibody Concentrations

GroupValue (Participants)
SOM230 LAR8
Other pre specified outcomeMean· at least 6 months

Health Related Quality of Life

GroupValue (units on a scale)Spread
SOM230 LAR58.628.9

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
SOM230 LARSOM230 LAR in a dosage of 60 mg i.m. once every 4 weeks0 / 167 / 1616 / 16

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
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Male or female patients aged ≥18 years * Diagnosis of thymoma as assessed by biopsy and/or szintigraphy * Inoperability of thymoma or loco-regional metastases. Inoperability is defined as at least adherence of the tumor to the neighbored organs, suspicious to infiltrate neighbored organs or local metastasis so that R0 resection can not be expected and /or local recurrence of thymic tumor * Tumor stage: Thymomas of all WHO based histological subtypes (WHO A, AB, B1, B2, B3) (Rosai, 1999; Travis 2004) at Masaoka stage II to IVa based on histological examination of resection specimens or core biopsies. * Patients with and without thymoma associated paraneoplastic syndrome. * Performance status 0,1, or 2 (ECOG) * Patients for whom written informed consent to participate in the study has been obtained Exclusion Criteria: * Patients having received radiolabeled somatostatin analogue therapy within the 6 months or any cytotoxic chemotherapy or interferon therapy within the 2 months prior to recording baseline symptoms * Patients who have undergone major surgery/surgical therapy for any cause within 1 month or surgical therapy of loco-regional metastases within the last 3 months before recording baseline symptoms * Patients who have received radiotherapy for any reason within the last 4 weeks and must have recovered from any side effects of radiotherapy before recording baseline symptoms * Patients who are not biochemically euthyroid * Diabetic patients on antidiabetic medications whose fasting blood glucose is poorly controlled as indicated by HbA1C \> 8% * Patients with symptomatic cholelithiasis * Patients who have congestive heart failure (NYHA Class III or IV), unstable angina, sustained ventricular tachycardia, ventricular fibrillation, clinically significant bradycardia, advanced heart block or a history of acute myocardial infarction within the six months preceding enrollment * Patients with QT related risk factor: QTcF at screening \> 450 msec * Patients with QT related risk factor: History of syncope or family history of idiopathic sudden death * Patients with QT related risk factor:Sudden or clinically significant cardiac arrhythmias * Patients with QT related risk factor: Risk factors for Torsades de Pointes such as hypokalemia, hypomagnesemia, cardiac failure, clinically significant / symptomatic bradycardia, or high-grade AV block * Patients with QT related risk factor: Concomitant disease(s) that could prolong QT such as autonomic neuropathy (caused by diabetes or Parkinson's disease), HIV, cirrhosis, uncontrolled hypothyroidism or cardiac failure * Patients with QT related risk factor: Concomitant medication(s) known to increase the QT interval * Patients with potassium \<3.0 mmol/L at study entry, magnesium \<0.4 mmol/L at study entry, calcium \<1.75 mmol/L at study entry, family history of long QT syndrome, and concomitant medications known to prolong the QT interval. If the electrolyte abnormalities are corrected prior to study commencement, the patient may become eligible for the trial. * Patients with liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis with serum bilirubin \> 1.5 X ULN, serum albumin \< 0.67 X LLN, and/or ALT or AST more than 2 X ULN for patients without liver Confidential - 20 - Amended Clinical Study Protocol v01 / Track Changes Study No. CSOM230CIC01T metastases or ALT or AST more than 5X ULN for patients with documented liver metastases * Patients with additional active malignant disease within the last five years (with the exception of basal cell carcinoma or carcinoma in situ of the cervix) * Patients with the presence of active or suspected acute or chronic uncontrolled infection or with a history of immunocompromise, including a positive HIV test result (ELISA and Western blot). A HIV test will not be required; however, previous medical history will be reviewed * Patients with abnormal coagulation (PT or APTT elevated by 30% above normal limits) * Patients with WBC \<2.5 X 109/L; Hgb \<10 g/dL; PLT \<100 X 109/L (patients with paraneoplastic pan-, leuco-, erythro- or thrombopenia can be included if this seems to be the only reason for pan-, leuco-, erythro- or thrombopenia) * Known hypersensitivity to somatostatin analogues or any component of the pasireotide or octreotide LAR or s.c. formulations * Patients who have any current or prior medical condition that may interfere with the conduct of the study or the evaluation of its results in the opinion of the investigator * Female patients who are pregnant or lactating, or are of childbearing potential and not practicing a medically acceptable method of birth control. Female patients must use a secure method of contraception if sexually active and the partner should use a condom. If oral contraception is used, the patient must have been practicing this method for at least two months prior to enrollment and must agree to continue the oral contraceptive throughout the course of the study, and for three months after the study has ended. Male patients who are sexually active are required to use condoms during the study and for three months afterwards as a precautionary measure (available data do not suggest any increased reproductive risk with the study drugs). Female partners of these male patients should use a secondary barrier contraception. * Patients who are currently part of or have participated in any clinical investigation with an investigational drug within 1 month prior to dosing * Patients with a history of non-compliance to medical regimens or who are considered potentially unreliable or will not be able to complete the entire study * Patient has received any other investigational agents within 28 days of first day of study drug dosing * Abnormal clinical laboratory values considered by the investigator to be clinically significant and which could affect the interpretation of the study results

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