Safety and Efficacy Trial of Danazol in Patients With Fanconi Anemia or Dyskeratosis Congenita
| Status: | Terminated |
|---|---|
| Conditions: | Anemia |
| Therapuetic Areas: | Hematology |
| Healthy: | No |
| Age Range: | 3 - Any |
| Updated: | 2/21/2019 |
| Start Date: | November 2009 |
| End Date: | May 2014 |
Phase I/II Dose Escalation Trial of Danazol in Patients With Fanconi Anemia or Dyskeratosis Congenita
Fanconi anemia (FA) and Dyskeratosis congenita (DC) are inherited bone marrow failure
syndromes. The current androgen treatments (e.g., oxymetholone) used to treat FA and DC can
cause unwanted masculinizing side effects, indicating a need for a different medication.
Danazol is a less potent androgen,and may therefore have fewer masculinizing side effects.
Danazol is currently approved by the Food and Drug Administration (FDA) for the treatment of
other diseases, but it has never been studied in patients with FA and DC.
The main purpose of this study is to see if danazol is a safe treatment for FA and DC.
Specifically,we would like to determine:
- the best dose of danazol;
- how fast hemoglobin (a protein that carries oxygen in the blood) levels rise in FA and
DC patients receiving danazol therapy; and
- the genetic pattern (known as expression profile) of certain cells in response to
danazol, which can predict how well people respond to the medication.
Subjects who enroll in the study will be treated with danazol for up to 24 weeks (about 6
months), and will have up to 11 study visits, including followup visits at 38 weeks (9
months) and 52 weeks (one year).
syndromes. The current androgen treatments (e.g., oxymetholone) used to treat FA and DC can
cause unwanted masculinizing side effects, indicating a need for a different medication.
Danazol is a less potent androgen,and may therefore have fewer masculinizing side effects.
Danazol is currently approved by the Food and Drug Administration (FDA) for the treatment of
other diseases, but it has never been studied in patients with FA and DC.
The main purpose of this study is to see if danazol is a safe treatment for FA and DC.
Specifically,we would like to determine:
- the best dose of danazol;
- how fast hemoglobin (a protein that carries oxygen in the blood) levels rise in FA and
DC patients receiving danazol therapy; and
- the genetic pattern (known as expression profile) of certain cells in response to
danazol, which can predict how well people respond to the medication.
Subjects who enroll in the study will be treated with danazol for up to 24 weeks (about 6
months), and will have up to 11 study visits, including followup visits at 38 weeks (9
months) and 52 weeks (one year).
Eligible patients with either Fanconi anemia (FA) or Dyskeratosis congenita (DC) will
initially receive danazol at a dose of 5 mg/kg/d orally, rounded to the nearest 100 mg. For
the first 8 weeks, the patient will be evaluated at weeks 2, 5, and 8 for hematologic
response (HR). If the patient shows a hematological response (either a hemoglobin or platelet
value no longer meeting blood cell count criteria for protocol inclusion in the absence of
recent transfusions)within the first 12 weeks on the initial dose, the study drug will be
continued at this dose for the next 6 weeks. If the patient fails to show any hematologic
response within the first 12 weeks, the dose will be escalated to 10 mg/kg/day for the next 6
weeks, and an additional monitoring visit will be required at week 14. If at week 18, the
patient fails to show any hematological response on the increased dose, the dose will be
increased to 15 mg/kg/day for another 6 weeks (not to exceed 800 mg/day), and an additional
monitoring visit will be required at week 20. At 24 weeks, if there is no response to this
dose the patient will be taken off study drug and classified as a treatment failure, and will
be monitored at weeks 38 and week 52). After week 24, if the patient continues to show a
response, however, the study drug may be continued at the discretion of their primary care
physician, with monitoring at weeks 38 and 52.
Should the patient lose the hematologic response on 5 or 10 mg/kg/day dosing at any point
within the first 18 weeks of treatment, the dose will be escalated to 10 or 15 mg/kg/day (not
to exceed 800 mg/day), respectively. The patient will continue to be evaluated at the next
visit. If after week 24 no hematologic improvement is seen, the patient is then taken off
study drug and monitored at weeks 38 and 52.
initially receive danazol at a dose of 5 mg/kg/d orally, rounded to the nearest 100 mg. For
the first 8 weeks, the patient will be evaluated at weeks 2, 5, and 8 for hematologic
response (HR). If the patient shows a hematological response (either a hemoglobin or platelet
value no longer meeting blood cell count criteria for protocol inclusion in the absence of
recent transfusions)within the first 12 weeks on the initial dose, the study drug will be
continued at this dose for the next 6 weeks. If the patient fails to show any hematologic
response within the first 12 weeks, the dose will be escalated to 10 mg/kg/day for the next 6
weeks, and an additional monitoring visit will be required at week 14. If at week 18, the
patient fails to show any hematological response on the increased dose, the dose will be
increased to 15 mg/kg/day for another 6 weeks (not to exceed 800 mg/day), and an additional
monitoring visit will be required at week 20. At 24 weeks, if there is no response to this
dose the patient will be taken off study drug and classified as a treatment failure, and will
be monitored at weeks 38 and week 52). After week 24, if the patient continues to show a
response, however, the study drug may be continued at the discretion of their primary care
physician, with monitoring at weeks 38 and 52.
Should the patient lose the hematologic response on 5 or 10 mg/kg/day dosing at any point
within the first 18 weeks of treatment, the dose will be escalated to 10 or 15 mg/kg/day (not
to exceed 800 mg/day), respectively. The patient will continue to be evaluated at the next
visit. If after week 24 no hematologic improvement is seen, the patient is then taken off
study drug and monitored at weeks 38 and 52.
Inclusion Criteria:
1. Patients must be diagnosed with FA that is documented by a positive test for increased
chromosomal breakage with mitomycin C or diepoxybutane. DC patients must have clinical
features consistent with the diagnosis, abnormally short lymphocyte telomeres < 1st
centile by flow-FISH evaluation, or mutation in one of the known DC genes (DKC1, TERT,
TERC, TINF2, NOP10, NHP2).
2. At least the following peripheral blood cytopenias: (without transfusion) Absolute
neutrophil count < 500/uL or Platelet count < 30,000/uL or Hemoglobin < 8.0 gm/dl
3. Negative pregnancy test by hCG testing, if of child-bearing potential.
4. Agreement to use a medically approved form of birth control, if of child-bearing
potential.
5. Signed informed consent by the patient or legally authorized representative.
6. Patients must be either 3 years of age or > 14 kg.
Exclusion Criteria:
1. Malignancy
2. Concurrent enrollment in any other study using an investigational drug.
3. Concurrent use of anticoagulants.
4. Use of androgen therapy within last three months.
5. Patients with liver disease as defined by SGOT, SGPT or bilirubin greater than the
upper limit of normal.
6. Patients with renal disease as defined by serum creatinine greater than the upper
limit of normal for age.
7. Patients less than either 3 years of age or 14 kg.
8. Patients who have HLA matched sibling donors.
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