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Phase I Safety Study of Clostridium Novyi-NT Spores in Patients With Treatment-refractory Solid Tumor Malignancies

Phase 1
18 Years
Open (Enrolling)
Solid Tumor Malignancies

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Trial Information

Phase I Safety Study of Clostridium Novyi-NT Spores in Patients With Treatment-refractory Solid Tumor Malignancies

Inclusion Criteria:

1. Diagnosis of an advanced solid tumor malignancy

2. History of prior treatment with at least one line of systemic anticancer therapy,
when an approved systemic therapy is available, and no curative option is available
for continued treatment.

3. Measurable disease as defined by RECIST 1.1 criteria.

4. At least 4 weeks has elapsed since the completion of major surgery and the patient is
fully recovered from this surgery and any post-surgical complications.

5. ECOG performance status of 2 or less.

6. Patient is at least 18 years of age

7. Patient is capable of giving informed consent.

8. Patient of childbearing potential (defined by the clinical sites' standards) is using
adequate birth control measures (e.g., barrier method with spermicide; intrauterine
device; implantable or injectable hormonal contraceptives; surgical sterilization)
for the duration of the study and will continue to use such precautions for 12 months
after receiving treatment.

9. Patient has no significant valvular disease (trace or mild valvular stenosis or
regurgitation is allowed).

10. Patient is able to stay within 45 minutes driving time of an emergency room for 28
days following discharge.

11. The patient has a caregiver for 28 days after dosing.

Exclusion Criteria:

1. Positive pregnancy test

2. Serum creatinine level > 1.5 x the upper limit of normal (ULN), chronic renal failure
requiring hemodialysis or peritoneal dialysis.

3. Patient has any of the following hematologic parameters: Platelet count equal to or
less than 100,000/mm3, Hemoglobin less than 9.0 g/dL, or an ANC less than 1,000 /mm3.

4. Oxygen saturation (Sp02) of less than 95% on room air.

5. Mean arterial blood pressure of less than 70 mmHg.

6. Glasgow Coma Score of less than 15.

7. Treatment with an investigational drug within the past 30 days or 5 half-lives of
that drug.

8. Documented evidence of primary brain malignancy or brain metastases.

9. Clinically significant ascites or clinical evidence or history of portosystemic
hypertension or cirrhosis.

10. Laboratory evidence of hepatic dysfunction indicated by any of the following:
bilirubin > 1.5 x the upper limit of normal, AST or ALT above 2.5X the upper limit
of normal, alkaline phosphatase above 2.5X the upper limit of normal or an INR
greater than 1.3.

11. Patient has a foreign body which in the opinion of the treating investigator could be
difficult to manage in case of infection (e.g. prosthetic hip).

12. Clinically significant pleural effusion.

13. Clinically significant pericardial effusion, circumferential pericardial effusion, or
any effusion greater than 1.0 cm at any location around the heart.

14. Need for ongoing treatment with an immunosuppressive agent.

15. History of solid organ transplantation (with the exception of a corneal transplant >
3 months prior to screening).

16. History of an ischemic insult in the previous 12 months (myocardial infarction,
cerebral vascular accident, ischemic tissue from injury, transient ischemic attack,
or clinically significant peripheral vascular disease).

17. Patient has a history of venous stasis resulting in venous stasis ulcers or > 2+

18. History of a significant medical illness deemed by the principal investigator or
local investigators as unsuitable for the trial - for example:

i. Symptomatic congestive heart failure; ii. Psychiatric Illness/Social Situation
that may make study dangerous; and iii. Unstable angina pectoris.

19. Asplenia.

20. Antibiotic allergies which would preclude treatment for a C. novyi-NT infection, in
the event that antibiotics are required.

21. Treatment with antibiotics within 2 weeks (14 days) of dosing.

22. Active and clinically significant systemic or localized infection.

Type of Study:


Study Design:

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

Outcome Measure:

Safety and tolerability of C. novyi-NT spore administration in patients with advanced solid tumor malignancies will be measured over a 7-day inpatient admission with routine labs and continuous adverse event assessments.

Outcome Time Frame:

2 years

Safety Issue:



United States: Food and Drug Administration

Study ID:




Start Date:

April 2011

Completion Date:

Related Keywords:

  • Solid Tumor Malignancies
  • Phase I
  • Metastatic Disease
  • Solid Tumor
  • Malignancy
  • Metastases
  • Clinical trial
  • Hypoxia
  • Necrosis
  • Neoplasms



Washington University School of MedicineSaint Louis, Missouri  63110
Sidney Kimmel Comprehensive Cancer Center at Johns HopkinsBaltimore, Maryland  21231-2410
Montefiore Medical CenterBronx, New York  10467-2490
University of Michigan Cancer CenterAnn Arbor, Michigan  48109