|Ingrid C Frey|
1 United States site
18 to 70 Years
Phase 1/Phase 2
– Subjects completing Study 19H0097 will first be screened for eligibility. Eligibility
criteria are identical with the exception of criteria 1.4, 2.2, and 2.3.p. If any of
the 15 subjects completing the 19H0097 study are unable to participate in or complete
the current extension study (defined as completing 24 weeks of treatment with study
drug to allow for assessment of the primary endpoint), then additional new subjects
na(SqrRoot) ve to mitapivat treatment
may be enrolled to replace them.
Subjects will enroll onto the study and undergo screening. Subjects who do not meet any of
the following criteria during screening will not receive the study intervention but will be
counted toward study accrual. Screen failures may be rescreened at a later time.
In order to be eligible to participate in this study, an individual must meet all of the
– 1.1 Have provided signed written informed consent prior to performing any study
procedure, including screening procedures.
– 1.2 Age between 18-70 years
– 1.3 Unequivocal diagnosis of HbSS confirmed by hemoglobin electrophoresis performed on
patients at least 90 days after a blood transfusion if previously transfused, or DNA
– 1.4 No transfusion in the 12 weeks prior to signing consent, or absence of Hb A on
hemoglobin analysis (by high-performance liquid chromatography; HPLC)
– 1.5 Have adequate organ function, as defined by:
– a. Serum aspartate aminotransferase (AST) <=2.5 x Upper Limit of Normal (ULN)
(unless the increased AST is assessed by the Investigator as due to hemolysis)
and alanine aminotransferase (ALT) <=2.5 x ULN.
- b. Serum creatinine <=1.25 x ULN. If serum creatinine is >1.25 x ULN, then
glomerular filtration rate (based on creatinine) must be >=60 mL/min.
– c. Absolute neutrophil count >=1.0 x 10^9power/L.
– d. Hemoglobin >= 7 g/dL
– e. Platelet count >=100 x 10^9/L.
– f. Activated partial thromboplastin time and international normalized ratio <=1.5 x ULN, unless the subject is receiving therapeutic anticoagulants. - 1.6 For women of reproductive potential, have a negative serum pregnancy test during the screening period. Women of reproductive potential are defined as sexually mature women who have not undergone a hysterectomy, bilateral oophorectomy, or tubal occlusion; or who have not been naturally postmenopausal (i.e., who have not menstruated at all for at least the preceding 1 year prior to signing informed consent unrelated to hormonal contraception). - 1.7 For women of reproductive potential as well as men and their partners who are women of reproductive potential, be abstinent as part of their usual lifestyle, or agree to use 2 effective forms of contraception from the time of giving informed consent, during the study, and for 28 days (both men and women) following the last dose of study treatment. An effective form of contraception is defined as hormonal oral contraceptives, injectables, patches, intrauterine or subdermal contraceptive implants, and barrier methods. - 1.8 Be willing to comply with all study procedures for the duration of the study.
– 2.1 Documented pyruvate kinase deficiency
– 2.2 Screening hemoglobin level of >= 11 g/dL
– 2.3 Have a significant medical condition that confers an unacceptable risk to
participating in the study, and/or that could confound the interpretation of the study
data. Such significant medical conditions include, but are not limited to the
– a. Poorly controlled hypertension (defined as systolic blood pressure [BP] >150
mmHg or diastolic BP >90 mmHg) refractory to medical management.
– b. History of recent (within 24 weeks prior to signing consent) decompensated
congestive heart failure; myocardial infarction or unstable angina pectoris;
hemorrhagic, embolic, or thrombotic stroke; deep venous thrombosis; or pulmonary
or arterial embolism.
– c. Cardiac dysrhythmias judged as clinically significant by the Investigator.
– d. Heart-rate corrected QT interval-Fredericia’s method (QTcF) >480 msec with the
exception of subjects with right or left bundle branch block.
– e. Clinically symptomatic cholelithiasis or cholecystitis. Prior cholecystectomy
is not exclusionary. Subjects with symptomatic cholelithiasis or cholecystitis
may be rescreened once the disorder has been treated and clinical symptoms have
– f. History of drug-induced cholestatic hepatitis.
– g. Iron overload sufficiently severe to result in a clinical diagnosis by the
Investigator of cardiac (e.g., clinically significant impaired left ventricular
ejection fraction), hepatic (e.g., fibrosis, cirrhosis), or pancreatic (e.g.,
– h. Have a diagnosis of any other congenital or acquired blood disorder, or any
other hemolytic process as defined by a positive direct antiglobulin test (DAT),
except mild allo-immunization as a consequence of transfusion therapy.
– i. Positive test for hepatitis B surface antigen or hepatitis C virus (HCV)
antibody (Ab) with signs of active hepatitis B or C virus infection. If the
subject is positive for HCVAb, a reverse transcriptase-polymerase chain reaction
test will be conducted. Subjects with hepatitis C may be rescreened after
receiving appropriate hepatitis C treatment.
– j. Positive test for human immunodeficiency virus 1 or 2 Ab.
– k. Active infection requiring any use of systemic antimicrobial agents
(parenteral or oral) or Grade >=3 in severity (per National Cancer Institute
Common Terminology Criteria for Adverse Events) within 8 weeks prior to signing
– l. Diabetes mellitus judged to be under poor control by the Investigator or
requiring >3 antidiabetic agents, including insulin (all insulins are considered
1 agent); use of insulin per se is not exclusionary.
– m. History of any primary malignancy, with the exception of: curatively treated
nonmelanomatous skin cancer; curatively treated cervical or breast carcinoma in
situ; or other primary tumor treated with curative intent, no known active
disease present, and no treatment administered during the last 3 years.
– n. Current or recent history of psychiatric disorder that, in the opinion of the
Investigator or Medical Monitor, could compromise the ability of the subject to
cooperate with study visits and procedures.
– o. Are currently enrolled in another therapeutic clinical trial involving ongoing
therapy with any investigational or marketed product or placebo. SCD subjects on
hydroxyurea or L-glutamine will also be considered, provided that they have been
on an unchanged dose of hydroxyurea or LGlutamine for 12 weeks prior to signing
consent. Use of the newer SCD therapies voxelotor or crizanlizumab will not be
permitted on this study, and subjects who have received voxelotor or
crizanlizumab in the 12 weeks prior to signing consent will be excluded.
– p. Have exposure to any investigational drug (other than the current drug,
mitapivat), device, or invasive procedure within 12 weeks prior to signing
consent. All non-investigational invasive procedures within 12 weeks of signing
consent may be considered as a potential exclusion criteria per the PI s
– q. Have had a prior bone marrow or stem cell transplant.
– r. Are currently pregnant or breastfeeding.
– s. Are currently receiving products that are strong inhibitors of CYP3A4/5 that
have not been stopped for (Bullet)5 days or a time frame equivalent to 5
half-lives (whichever is longer), or strong inducers of CYP3A4 that have not been
stopped for (Bullet)28 days or a time frame equivalent to 5 half-lives (whichever
is longer), prior to signing consent.
– t. Are currently receiving hematopoietic stimulating agents (e.g.,
erythropoietins, granulocyte colony stimulating factors, thrombopoietins) that
have not been stopped for a duration of at least 90 days prior to signing
– u. Have a history of allergy to sulfonamides if characterized by acute hemolytic
anemia, drug-induced liver injury, anaphylaxis, rash of erythema multiforme type
or Stevens-Johnson syndrome, cholestatic hepatitis, or other serious clinical
– v. Have a history of allergy to mitapivat or its excipients (microcrystalline
cellulose, croscarmellose sodium, sodium stearyl fumarate, and mannitol).