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A Phase I, Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Sodium Stibogluconate in Combination With Interferon Alpha-2b for Patients With Advanced Malignancies

Phase 1
18 Years
Not Enrolling
Advanced Cancer, Solid Tumors

Thank you

Trial Information

A Phase I, Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Sodium Stibogluconate in Combination With Interferon Alpha-2b for Patients With Advanced Malignancies

Sodium stibogluconate is a drug that is able to block an enzyme in the cells that is
responsible for cell growth. By blocking this enzyme, it may be able to prevent cancer cells
from multiplying.

Interferon alfa-2b is a drug that activates an immune response to infections in the body. By
triggering an immune response, this drug may help to prevent some cancer cells from growing
and multiplying. You will receive treatment with both sodium stibogluconate and interferon
alfa-2b, because sodium stibogluconate may improve the effectiveness of interferon in
treating the cancer.

Participants will be enrolled in groups of 3 on this study, and the doses of the study drugs
will be escalated for each group. This means that each new group of 3 participants will get
a higher dose of the study drugs than the group before them. This will continue until the
highest tolerable dose combination is found.

Once the highest tolerable dose has been found, up to an additional 9 participants, called
the expansion group, will receive study drug at that dose. Your doctor will tell you if you
are in the expansion group.

If you are found to be eligible to take part in this study, you will go to the clinic to
start treatment. During Cycle 1, you will be given sodium stibogluconate once a day by vein
during Days 1-5. On Days 8-12, you will be given sodium stibogluconate once a day by vein,
and you will be given interferon alfa-2b for 3 days by injection just under the skin on Days
8, 10, and 12. For every cycle after Cycle 1, you will be given sodium stibogluconate once a
day by vein during Days 1-5 and 8-12, and you will be given interferon alfa-2b for 3 days by
injection just under the skin on Days 1, 3,5, 8, 10, and 12. Treatment cycles will last
about 3 weeks (2 weeks on treatment, followed by 1 week off treatment).

During each visit to the clinic, you will be asked how you are feeling, and your vital signs
will be measured. You will have a complete physical exam the first day of every cycle. On
Days 1, 8, and 12 of every cycle, you will have a urine test to check the function of your
kidneys, and blood (about 3 teaspoons) will be drawn for routine tests. On Days 1, 8, and 12
of every cycle and during your last study visit, you will have an additional blood draw
(about 5 teaspoons) for immunological testing (to help researchers learn how your body
fights disease) before treatment. On Days 1, 5, 8, and 12 of every cycle, you will have an
ECG after you receive treatment.

At some time during the week before Day 1 of Cycle 1 and on Day 12 of Cycle 2, you may have
a tumor biopsy to check the status of the disease before you receive the study drug. To
perform a tumor biopsy, the affected area is numbed with anesthetic, and a small amount of
tumor tissue is withdrawn through a large needle. Your doctor will tell you if this may be

On Days 1, 2, 9, 12, and 13 of Cycle 1, you will have blood drawn (about 1 teaspoon each)
for PK testing. On Days 1, 8, and 12, the PK testing will be done before, 30 minutes after,
and 2 hours after you receive the study drug. On Days 2 and 9, the PK testing will be done
before treatment. On Day 13, the PK testing will be done 24 hours after you received
treatment on Day 12.

After Cycle 1, you will be scheduled to return to the clinic in 10 days to receive treatment
for Cycle 2, which will follow in the same manner as Cycle 1.

At the end of Cycle 2 and every even-numbered cycle (Cycles 4, 6, 8, and so on) after that,
you will have imaging studies, such as x-rays and CT scans, to check the status of your

If the disease does not get worse and you do not experience any intolerable side effects
after Cycle 1, you will continue on to Cycle 2, and so on. If at any time the disease gets
worse or you experience any intolerable side effects, you will be taken off this study.

This is an investigational study. Sodium stibogluconate is not FDA approved or commercially
available. It is authorized for use in research only. Interferon alfa-2b is approved by the
FDA for the treatment of some types of cancers (solid tumors). The combination of these
drugs is investigational in this study. Their use together is authorized for use in
research only.

However, if sodium stibogluconate becomes commercially available while you are still on
study. Up to 54 patients will take part in this multicenter study. Up to 35 will be enrolled
at M. D. Anderson.

Inclusion Criteria:

1. Patients who sign a written informed consent document and are able to comply with the
study protocol for the duration of the study.

2. Patients who have a histologically or cytologically confirmed diagnosis malignancy
(patients with measurable or non-measurable disease) who have progressed following
effective therapy or for which no effective therapy exists.

3. Patients who are greater than or equal to 18 years of age.

4. Patients who have an Eastern Cooperative Oncology Group (ECOG) Performance Status of

5. Patients who have an estimated life expectancy of 3 months.

6. Patients who have a normal cardiac ejection fraction, >50% estimated by 2 D
Echocardiogram or MUGA.

7. Patients who have adequate organ function as indicated by the following laboratory
values obtained within 10 days prior to the first dose of SSG: Granulocytes>/=1,500
microliter, Platelets>/= 100,000 microliter, Hemoglobin >/=9.0 g/dL,Creatinine (Cr)
Aspartate aminotransferase (AST) <2.5 * ULN or <5.0 * ULN with liver metastases,
Alanine aminotransferase (ALT)<2.5 * ULN or <5.0 * ULN with liver metastases.

Exclusion Criteria:

1. Patients on concurrent immunotherapy, including IFN therapy (prior therapy is allowed
if >/= 4 months since immunotherapy).

2. Patients who have received investigational drugs including immunotherapy, gene
therapy, hormone therapy, biologic therapy, radiation therapy, chemotherapy, or had
major surgery within 3 weeks of study enrollment

3. Patients who have not recovered from acute toxicity of previous therapy prior to

4. Patients with medically uncontrolled cardiovascular illness, unstable angina,
congestive heart failure, history of myocardial infarction, electrocardiogram (ECG)
abnormalities suggestive of cardiac conduction delay (QTc >0.47 seconds), history of
atrial fibrillation or flutter, or other serious clinically significant cardiac

5. Patients who have an active, uncontrolled systemic infection considered
opportunistic, life threatening, or clinically significant.

6. Pregnant or lactating women, and fertile women or men unless surgically sterile or
using effective contraception; All female patients of childbearing potential or < 1
year postmenopausal must have a negative beta human chorionic gonadotropin (βhCG)
pregnancy test at baseline and be practicing a medically acceptable method of birth
control (oral contraceptives for at least 3 months, implantation of an intrauterine
device at least 2 months, or barrier methods [e.g. vaginal diaphragm, vaginal sponge,
or condom with spermicidal jelly]). These must be continued for 3 months after study

7. Patients who use daily glucocorticoids except for physiological replacement.

8. Patients who are known to be positive for Hepatitis B surface antigen, Hepatitis C or
human immunodeficiency virus (HIV).

9. Patients with prior history of solid organ allografts or allogeneic bone marrow

10. Patients who have a psychiatric disorder(s) that would interfere with consent, study
participation, or follow-up.

11. Patients who have any other severe concurrent disease, which, in the judgment of the
investigator, would make the patient inappropriate for entry into this study.

12. Patient who have symptomatic or untreated central nervous system metastases.

13. Patients taking the following medications will not be eligible: Amiodarone
(Cordarone); Disopyramide (Norpace); Dofetilide (Tikosyn); Procainamide (Procanbid,
Pronestyl); Quinidine (Quinaglute); Sotalol (Betapace); Erythromycin; Azithromycin
(Z-pack), cont'd

14. Clarithromycin (Biaxin); Pentamidine (Pentacarinat); Trimethoprim-sulfamethoxazole
(Bactrim); Bepridil (Vascor); Phenothiazines-prochlorperazine (Compazine),
promethazine (Phenergan), chlorpromazine (Thorazine) or any antipsychotic medication;
Butyrophenones-Haloperidol (Haldol), cont'd

15. Risperidone (Risperdal); Tricyclic or tetracyclic antidepressants—imipramine
(Tofranil), amitriptyline (Elavil), desipramine (Norpramin), nortriptyline (Pamelor);
Monoamine oxidase inhibitors; High dose methadone; Arsenic trioxide; Dolasetron
(Anzemet); Any herbal preparations; or • Chronic need for colony stimulating factors
(i.e., GM-CSF), erythropoietin use is permitted.

16. Patients with a history of hypersensitivity to IFN a-2b or SSG or any of their

Type of Study:


Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Maximum tolerated dose (MTD) of SSG in combination with IFN alpha2b

Outcome Description:

MTD defined as the highest dose at which no dose limiting toxicity (DLT) occurs.

Outcome Time Frame:

Continuous assessment with each 3 week cycle

Safety Issue:


Principal Investigator

Aung Naing, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

M.D. Anderson Cancer Center


United States: Food and Drug Administration

Study ID:




Start Date:

September 2006

Completion Date:

February 2010

Related Keywords:

  • Advanced Cancer
  • Solid Tumors
  • Advanced Malignancies
  • Solid Tumors
  • Melanoma
  • Renal Cell Carcinoma
  • Phase I Studies
  • Sodium Stibogluconate
  • Interferon Alpha-2b
  • Intron A
  • SSG
  • Neoplasms



U.T.M.D. Anderson Cancer CenterHouston, Texas  77030
University of New MexicoAlbuquerque, New Mexico  87131