Trial Search Results

Phase 1/2 Dose Escalation Study in Patients With Relapsed or Refractory Waldenstrom's Macroglobulinemia

The purpose of this study is to see if IMO-8400 is safe and effective in the treatment of subjects with relapsed or refractory Waldenström's Macroglobulinemia following conventional treatment.

Recent reports have identified a specific oncogenic mutation L265P of the MYD88 gene in approximately 90% of the patients with Waldenström's macroglobulinemia. MYD88 is a key linker protein in the signaling pathway of Toll Like Receptors (TLRs) 7, 8, and 9, and IMO-8400 is an oligonucleotide specifically designed to inhibit TLRs 7,8, and 9. The scientific hypothesis for use of IMO-8400 to treat patients with Waldenström's macroglobulinemia depends on the inhibition of mutant MYD88 signaling in the TLR pathway, thereby interrupting the proliferation of cell populations responsible for the propagation of the disease.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Idera Pharmaceuticals, Inc.

Stanford Investigator(s):

Intervention(s):

  • Drug: IMO-8400

Phase:

Phase 1/Phase 2

Eligibility


Inclusion Criteria:

Patients must have a diagnosis of relapsed Waldenstrom's Macroglobulinemia.

In addition to the above, key inclusion and exclusion criteria are listed below.

Inclusion Criteria:

   1. At least 18 years of age.

   2. Agree to use contraception

   3. Hemoglobin ≥ 7.5 g/dL, - Absolute neutrophil count ≥ 1.0 x 109/L (1000/mm3), -
   Platelets ≥ 50,000/μL

Exclusion Criteria:

   1. Is nursing or pregnant

   2. Has BMI > 34.9 kg/m2.

   3. Has a positive test for human immunodeficiency virus (HIV-1 or -2) hepatitis C virus
   (HCV) or hepatitis B surface antigen (HBsAg).

   4. Receiving chronic systemic corticosteroid therapy > 20 mg of prednisone daily.

   5. Being treated with other anti-cancer therapies (approved or investigational).

   6. Has, at the initiation of study drug, received cytotoxic chemotherapy or a Bruton's
   tyrosine kinase (BTK)-inhibitor (e.g. ibrutinib) within the past 3 weeks or rituximab
   within the past 2 months

   7. Has an active infection requiring systemic antibiotics.

   8. Has had surgery requiring general anesthesia within 4 weeks of starting the study.

   9. Has autoimmune cytopenia (anemia, thrombocytopenia, leukopenia).

10. Has heart failure of Class III or IV.

11. Has sensory or motor neuropathy limiting daily activities.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting