The Use of Trifluoperazine in Transfusion Dependent DBA

• Status: Terminated
• Trial end date: 2021-10-13
• Target enrollment: 0
• Participant gender: All

Summary

Diamond Blackfan anemia (DBA) is a rare inherited pure red cell aplasia. The two main non-stem cell transplant therapeutic options are corticosteroids and red blood cell (RBC) transfusions. About 80% of DBA patients initially respond to corticosteroids, however, half of the patients cannot continue due to side effects or loss of response. These patients are then typically dependent on RBC transfusions throughout life. Each of these treatments is fraught with many side effects and significant morbidity and mortality are potential consequences of hematopoietic stem cell transplantation (SCT). The majority of individuals with DBA have mutations in genes encoding structural proteins of the small or large ribosomal subunit leading to deficiency of the particular ribosomal protein (RP). Using the RP deficient zebrafish embryo model, high throughput drug screens have demonstrated a strong hematologic response to several calmodulin inhibitors. One of these chemicals is trifluoperazine (TFP). TFP treatment of a mouse model of DBA also increased the red blood cell count and the hemoglobin (Hb) levels in the mice. TFP is a FDA-approved typical antipsychotic agent that has been available since 1958 with a well-known safety profile. In the United States, TFP is approved for the short-term treatment of generalized non-psychotic anxiety; treatment or prevention of nausea and vomiting of various causes; and, management of psychotic disorders.

This study aims to determine the safety/tolerability of TFP in adult subjects with DBA. TFP's expected dose-limiting toxicity is primarily neurologic (extrapyramidal) when used long-term at typical anti-psychotic doses (range 10-50 mg daily). Non-neurologic adverse effects in subjects with DBA have not been investigated. We will perform a dose escalation study to define the safety and tolerability of lower doses of this agent in subjects with DBA. To mitigate the potential risks of administering TFP to this new population, we will (1) start dosing at dose levels well below those prescribed for psychosis, (2) dose escalate to a maximum of 10 mg daily (the lowest dose typically prescribed for psychosis), and (3) perform weekly safety monitoring. Given the positive signal in DBA animal models and the 60-year clinical experience with higher doses of TFP, this drug warrants a trial in humans to assess tolerability in DBA.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Adrianna Vlachos
• Treatments: Trifluoperazine

Criteria

Inclusion Criteria:

• Men and women age: 18 years and <65 years of age.

• Weight: ≥45 kilograms.

• DBA diagnosed according to the DBA criteria (Vlachos, 2008)

• RBC transfusion-dependence (defined as 2 units packed RBCs per 28 days averaged over 84 days [12 weeks] prior to study entry)

• Calculated creatinine clearance > 30 mL/min

• Karnofsky performance status scale score ≥ 70

• Female subjects of childbearing potential must have a negative serum pregnancy test and use highly effective methods of birth control during the study

• Male subjects must agree to use a latex condom during any sexual contact with females of childbearing potential while participating in the study

• Agreement to adhere to the study visit schedule, understand and comply with all protocol requirements.

Exclusion Criteria:

• Liver: aspartate aminotransferase (AST) > 5 x the upper limit of normal (ULN), alanine aminotransferase (ALT) >5 x ULN, or bilirubin > 5 x ULN

• Heart disease (New York Heart Association classification of ≥ 3)

• History of angina

• Uncontrolled hypertension

• Subjects currently responsive to corticosteroids for treatment of DBA.

• Treatment with another investigational drug or device <56 days pre-study entry.

• Pregnant or lactating females

• Any history of severe allergic reaction requiring the use of epinephrine

• Known hypersensitivity to the study drug or other phenothiazines

• History or presence of extrapyramidal signs

• History of cancer