Safety and Pharmacokinetic Study of Escalating Multiple Doses of an Iron Chelator in Patients With Iron Overload

Phase 1

Completed

• Conditions: Transfusional Iron Overload; Beta-thalassemia
• Interventions: Drug: FBS0701

• Registration Number: NCT01039636
• Lead Sponsor: FerroKin BioSciences, Inc.

Brief Summary

The purpose of this research study is to study the safety of increasing doses of FBS0701, and to see how quickly the study medication is absorbed and how quickly it disappears from the bloodstream. FBS0701 is a new, oral iron chelator - a medication taken by mouth that increases the body's elimination of iron. Iron chelators are used in patients who develop iron overload from their transfusions. Four increasing doses of FBS0701 will be tested during this study. The study will start with the lowest dose given to 4 patients (3 mg/kg/day. The next group of 4 patients will receive the next high dose (8mg/kg/day only after the results of the first 4 patients are examined and it is determined safe to continue. Participating patients will take the study medication for 7 days and be followed for 28 days after their last dose to determine if they have any reactions to the study medication - therefore a total of 35 days on study. Patients will need to give up to 17 blood samples over the screening period and first 15 days of the study (a total of about 9 tablespoons). Patients will not need to stay overnight in the clinic but will need to visit the clinic 10 times for screening and on-study visits over the 35 days. Patients currently taking an iron chelator will need to stop that treatment for up to 22 days (up to 5 days before they start the study and for 15 days during the study). The results of this study will be helpful in determining the safety of the drug and the best doses of FBS0701 to be used in the next study which will assess the effectiveness of this new iron chelator.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-11
• Study First Submitted: 2009-12-23
• Study First Submitted QC: 2009-12-23
• Study First Posted: 2009-12-25
• Primary Completion: 2010-12
• Status Verified: 2011-01
• Last Update Submitted: 2012-02-08
• Last Update Posted: 2012-02-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• At least 18 years old
• Transfusion dependent (at least 8 transfusions per year) with transfusional iron overload needing treatment with deperoxamine, deferasirox or deperiprone.
• Willing to discontinue current iron chelation therapy for 2-5 days prior to enrollment and for a total of up to 3 weeks
• Willing to fast after midnight prior to each dose
• Serum ferritin greater than 400ng/ml
• Liver iron concentration greater than or equal to 1.5 mg iron. (determined by MRI or SQUID within 12 months prior to enrollment)
• Cardiac iron greater than or equal to 12 milliseconds (determined by MRI t2* within 18 months prior to enrollment)
• Mean of last 3 pre-transfusion hemoglobin values must be greater than or equal to 7.5 g/dl
• Agrees to use approved contraception from Screening and until 30 days after last administration of study drug. Abstinence OK.

Exclusion Criteria

• Principal Investigator considers patient unfit for study after conducting a medical review, physical examination and other screening assessments.
• Non-elective hospitalization with past 30 days
• Evidence of clinically relevant oral, cardiovascular, gastrointestinal, hepatic, renal, endocrine, pulmonary, neurologic, psychiatric or skin disorder.
• Evidence of significant renal insufficiency; serum creatine above upper limit of normal or proteinuria greater than 2 gm per day or calculated creatinine clearance of less than or equal to 60ml/min
• Platelet count below 150,000,000/ml and/or absolute neutrophil count less then 1500/mm3
• Alkaline phosphatase or AST greater than 5 times the upper limit of normal or ALT greater than 4 times the upper limit of normal
• Female patients who are pregnant or lactating
• Use of any investigational agent within the last 30 days

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
FBS0701 - 5 escalating doses	FBS0701	5 escalating doses of FBS0701 in 5 cohorts of 4 patients each.

Primary Outcome Measures

Name	Time	Method
Safety and tolerability by AEs, Physical Exam, Clinical Laboratory assessments	35 days (7 days treatment and 28 days follow up)
Steady state plasma level and half-life of FBS0701	7 days of dosing

Secondary Outcome Measures

Name	Time	Method
Urinary excretion of iron	7 days of dosing

Trial Locations

Locations (5)

Children's Hospital of Boston; 🇺🇸 Boston, Massachusetts, United States

Siriraj Hospital, Mahidol University; 🇹🇭 Bangkok, Thailand

Royal Adelaide Hospital; 🇦🇺 Adelaide, Australia

Children's Hospital of Oakland; 🇺🇸 Oakland, California, United States

Children's Hospital of Philadelphia; 🇺🇸 Philadelphia, Pennsylvania, United States