Phase 2a Desipramine in Small Cell Lung Cancer and Other High-Grade Neuroendocrine Tumors

Stopped early · Phase 2

Conditions studied: Small Cell Lung Cancer (SCLC), Neuroendocrine Tumors

In brief

Intrapatient dose escalation study of desipramine in subjects with small cell lung cancer (SCLC) and other high-grade neuroendocrine tumors.

Key facts

Study ID

NCT01719861

Run by

Joel Neal

People needed

6

Starts

2012-10-01

Expected to finish

2015-05-01

Last updated by the study team

2017-04-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Metastatic small-cell lung cancer
• Metastatic high-grade neuroendocrine carcinoma of any organ system (high-grade defined by Ki-67 ≥ 20% and/or ≥ 20 mitoses/10 (HPF).
• Received at least one line of prior chemotherapy treatment for metastatic disease.
• Daily chemotherapy must be completed ≥ 2 weeks prior to registration
• Weekly chemotherapy must be completed ≥ 2 weeks prior to registration
• Chemotherapy every 2 weeks must be completed ≥ 3 weeks prior to registration
• Chemotherapy every 3 weeks must be completed ≥ 4 weeks prior to registration
• ECOG Performance Status 0 to 2
• Measurable disease by RECIST 1.1 criteria
• Age at least 18 years
• Estimated life expectancy at least 3 months
• Absolute neutrophil count ≥ 1,500/ mm³
• Platelets ≥ 100,000/mm³
• Hemoglobin ≥ 9 g/dL
• Total bilirubin ≤ 1.5 mg/dL, OR ≤ 2 X ULN if tumor involves the liver
• AST(SGOT)
• ALT(SGPT) ≤ 3 X ULN
• Creatinine ≤ 1.5 X ULN
• Creatinine clearance ≥ 45 mL/min/1.73m²) for patients with creatinine levels above institutional normal
• QT interval corrected using Fridericia's method (QTcF) < 450 msec (males) or < 470 msec (females)
• PR < 240 msec
• QRS < 100 msec
• Brain metastases must be asymptomatic and have been adequately treated with radiation finishing at least 1 week prior to initiation of study treatment.
• Ability to understand and the willingness to sign a written informed consent document.

You may not qualify if…

• Clinically-significant ventricular arrhythmia including cardiac arrest
• Myocardial infarction from coronary artery disease within 3 months of study enrollment
• Implantable pacemaker or implantable cardioverter defibrillator
• NYHA Class III or greater congestive heart failure
• Other clinically-significant cardiac disorders
• Family history of long QT syndrome.
• Concomitant or expected treatment with strong inhibitors of cytochrome p450 CYP2D6, specifically including Bupropion; Fluoxetine; or Paroxetine (must be discontinued at least 2 weeks or 5-half lives prior to the initiation of desipramine, whichever is shortest, except fluoxetine which requires at least a 5-week washout period).
• Use of medications known to increase risk of torsades de pointes, including Amiodarone; Arsenic trioxide; Astemizole; Azithromycin; Bepridil; Chloroquine; Chlorpromazine; Cisapride; Citalopram; Clarithromycin; Disopyramide; Dofetilide; Domperidone; Droperidol; Erythromycin; Flecainide; Halofantrine; Haloperidol; Ibutilide; Levomethadyl; Mesoridazine; Methadone; Moxifloxacin; Pentamidine; Pimozide; Probucol; Procainamide; Quinidine; Sotalol; Sparfloxacin; Terfenadine; Thioridazine; Vandetanib
• Other anti-depressant or anti-psychotic medications including selective serotonin re-uptake inhibitors (SSRIs); other tricyclic, monoamine oxidase inhibitors (MAOIs); serotonin-norepinephrine reuptake inhibitors (SNRIs, typical or atypical anti-psychotic)
• Metoclopramide (Reglan) because of increased risk of extrapyrimidal symptoms and neuroleptic malignant syndrome
• Symptomatic orthostatic hypotension despite adequate volume resuscitation.
• Medical history of narrow angle glaucoma
• Bipolar disorder, ongoing or active within the last 5 years
• Suicidal ideation, ongoing or active within the last 5 years
• Suicide attempt, ongoing or active within the last 5 years
• Pregnancy
• Breastfeeding
• Receiving any other investigational agents
• Any other serious or unstable concomitant systemic disorder that in the opinion of the investigator is incompatible with the clinical study

Where it is running

• Stanford University Cancer Institute — Stanford, California, United States

Full record on ClinicalTrials.gov

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