High Dose Ascorbic Acid for Plasma Cell Disorders

Christopher Strouse

Status and phase: Completed; Phase 1

Conditions: Multiple Myeloma

Treatments: Other: Ascorbate; Drug: Melphalan

Study type: Interventional

Funder types: Other

Identifiers

NCT03602235

201804754

Details and patient eligibility

About

This is a Phase I single-arm open-label clinical study primarily assessing the safety and secondarily, the relative efficacy of low dose melphalan + high dose ascorbate acid (HDAA) in relapsed refractory patients with multiple myeloma.

Full description

This is a phase 1 study for patients with relapsed refractory multiple myeloma. Patients will receive a 15-gram test dose, and a maximum of 3 cycles, each composed of 4 doses of high-dose ascorbic acid (HDAA) and 2 doses of melphalan. This study will enroll 9 patients with relapsed refractory multiple myeloma. The starting dose of ascorbic acid will be 50 grams. Using a 3+3 dose escalation, the dose will potentially increase to 75 grams then 100 grams.

Enrollment: 6 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Subject has provided informed consent.

• Diagnosis of multiple myeloma per IMWG criteria(26)

• Patients must have progressive disease following 3 or more prior lines of therapy.

  • Prior treatment must include a proteasome inhibitor, an immunomodulatory agent (IMiD), and an anti-CD38 monoclonal antibody.
  • Patients must not be candidates for regimens known to provide clinical benefit in relapsed or refractory multiple myeloma based on the investigator's judgement.
  • If a patient declines such therapy, this must be recorded in the study files. 4. Subjects must have measurable disease, including at least one of the criteria below:
  • SPEP demonstrating M-protein quantities ≥ 0.5 g/dl
  • UPEP demonstrating monoclonal protein ≥ 200 mg/24hr
  • Involved serum free light chain levels > 100 mg/L and an abnormal kappa/lambda (κ/λ)ratio
  • For patients with immunoglobulin class A (IgA) myeloma whose disease can only be reliably measured by quantitative immunoglobulin measurement, a serum IgA level ≥ 500 mg/dl will qualify as measurable disease
  • Non-secretory participants are eligible provided the participant has > 20% bone marrow plasmacytosis

• Adequate organ function:

  • Absolute neutrophil count (ANC) ≥ 1.0 x 10^9/L without growth factor support for 7 days
  • Platelets (plt) ≥ 50 x 10^9/L without transfusion for 7 days.
  • Hemoglobin ≥ 8.0 g/dl, transfusion support permitted
  • Aspartate aminotransferase (AST/SGOT) and alanine aminotransferase (ALT/SGPT) ≤ 3.0x upper limit of normal (ULN)
  • Serum bilirubin ≤ 1.5 x ULN
  • Estimated serum creatinine clearance of ≥ 45 mL/min using the Cockcroft-Gault equation or directly calculated from the 24-hour urine collection method.
  • International normalized ratio (INR) < 1.5 x ULN and partial thromboplastin time (PTT) < 1.5 x ULN
  • Left Ventricular Ejection Fraction by ECHO or MUGA of ≥ 40%.
  • Participants must have a performance status of 0-2 based on ECOG criteria.
  • For people of child bearing potential negative serum or urine pregnancy test (sensitivity of at least 25 mIU/mL) at screening

Exclusion Criteria

• Known hypersensitivity or allergy to ascorbic acid or melphalan
• Participants must not have a concurrent malignancy unless it can be adequately treated by non- chemotherapeutic intervention. Participants may have a history of prior malignancy, provided they have not had any chemotherapy within 365 days of study entry AND their life expectancy exceeds 5 years with respect to the concurrent malignancy at the time of study entry.
• Participants must not have life-threatening comorbidities.
• Known human immunodeficiency virus(HIV) disease (requires negative test for clinically suspected HIV infection).
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, recent (within 6 months) myocardial infarction, uncontrolled or symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled hypertension on appropriate therapy or psychiatric illness/social situations that would limit compliance with study requirements.
• Concurrent use of Coumadin (warfarin)
• Patients with G6PD deficiency
• Patients with a history of oxalate renal stones or a known history of multiple renal stones
• Diabetic patients who rely on a glucometer to dose insulin as ascorbate can interfere with glucometer readings

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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6 participants in 1 patient group

Low dose melphalan + high dose ascorbate acid (HDAA)

Experimental group

Description:

Patients will receive a test dose of 15g of HDAA prior to starting treatment dose. This will be mainly to rule out allergic reactions. HDAA + Melphalan: HDAA on day 1 and day 4 in combination with melphalan 12.5 mg/m2, followed by 2 additional doses of HDAA on day 2 and day 5. A 3 + 3 cohort method will be used for this study. After successfully completing the test dose, subjects will receive 50gms, 75gms and 100gms of ascorbate per infusion in 3 different cohorts. Dose modifications are not made for weight or body surface area.

Treatment:

Drug: Melphalan

Other: Ascorbate