Safety of Fresolimumab in the Treatment of Osteogenesis Imperfecta
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Osteogenesis Imperfecta (OI) is a rare disorder that causes bones to break easily. People with OI may have broken bones with little or no trauma, dentinogenesis imperfecta (DI), and, in adult years, hearing loss. It is seen in both genders and all races. OI can range from very severe to very mild. Individuals with the most severe type of OI may die at birth. People with severe OI who survive may have bowed arms and legs, very short stature and be unable to walk. People with the mildest form of OI may only break bones occasionally and have normal height and lifespan. Breaks can occur in any bone, but are most common in the arms and legs. The current standard-of-care for severe types of OI involves the use of IV medications (bisphosphonates) and surgery to put rods in bones to strengthen them. These therapies, although often life-saving, are new and very little is known about their long-term effects on bone and other body systems.
TGF-β is a protein important in bone formation. Studies have shown that increased TGF-β activity leads to lower bone mass and strength and increased fractures. Fresolimumab is an antibody that can silence TGF-β . In studies with mice with OI, it has been shown that silencing TGF-β can lead to higher bone mass, quality and strength.
Tarixlər
| Son Doğrulandı: | 03/31/2020 |
| İlk təqdim: | 10/12/2016 |
| Təxmini qeydiyyat təqdim edildi: | 02/20/2017 |
| İlk Göndərmə: | 02/23/2017 |
| Son Yeniləmə Göndərildi: | 04/06/2020 |
| Son Yeniləmə Göndərildi: | 04/07/2020 |
| Həqiqi Təhsilin Başlama Tarixi: | 11/14/2017 |
| Təxmini İlkin Tamamlanma Tarixi: | 07/31/2022 |
| Təxmini İşin Tamamlanma Tarixi: | 09/30/2022 |
Vəziyyət və ya xəstəlik
Müdaxilə / müalicə
Drug: Fresolimumab
Faza
Qol Qrupları
| Qol | Müdaxilə / müalicə |
|---|---|
| Experimental: Stage 1 Low dose There are a total of 6 study visits within approximately a 6 month timespan. Investigators will evaluate the safety of a single administration of fresolimumab in adult patients with OI. Subjects will receive a single-dose of 1 mg/kg of fresolimumab (n=4).
At each study visit, the participant may have the following testing done:
Physical exam
Vitals
Blood draw for safety labs, pharmacokinetics, etc
If the participant is female, she will have a pregnancy test
EKG
DXA
Infusion of the study drug | |
| Experimental: Stage 2 High dose There are a total of 6 study visits within approximately a 6 month timespan. Investigators will evaluate the safety of a single administration of fresolimumab in adult patients with OI. Subjects will receive a single-dose of 4 mg/kg of fresolimumab (n=4).
At each study visit, the participant may have the following testing done:
Physical exam
Vitals
Blood draw for safety labs, pharmacokinetics, etc
If the participant is female, she will have a pregnancy test
EKG
DXA
Infusion of the study drug | |
| Experimental: Stage 2 Repeat dose every 6 months Fresolimumab will be administered every six months for a total treatment period of 12 months (n=4). The dose to be administered (1 or 4 mg/kg) will be chosen after completion of Stage 1. The primary Stage 2 endpoint will be safety measures assessed over 12 months. The secondary endpoints will be changes in markers of bone remodeling, bone mineral density, estimated strength.
At each study visit, participants may have the following testing done:
Physical exam
Vitals
Blood draw for safety labs, pharmacokinetics, etc
If the participant is female, she will have a pregnancy test
EKG
DXA
Infusion of the study drug
Skeletal survey
Peripheral quantitative CT (pQCT) of the forearm
Quality of Life Surveys
Pulmonary function test
Walk test | |
| Experimental: Stage 2 Repeat doses every 3 months Fresolimumab will be administered every three months for a total treatment period of 12 months (n=4). The dose to be administered (1 or 4 mg/kg) will be chosen after completion of Stage 1. The primary Stage 2 endpoint will be safety measures assessed over 12 months. The secondary endpoints will be changes in markers of bone remodeling, bone mineral density, estimated strength.
At each study visit, participants may have the following testing done:
Physical exam
Vitals
Blood draw for safety labs, pharmacokinetics, etc
If the participant is female, she will have a pregnancy test
EKG
DXA
Infusion of the study drug
Skeletal survey
Peripheral quantitative CT (pQCT) of the forearm
Quality of Life Surveys
Pulmonary function test
Walk test |
Uyğunluq Kriteriyaları
| Təhsil üçün uyğun yaşlar | 18 Years Üçün 18 Years |
| Təhsilə Uyğun Cinslər | All |
| Sağlam Könüllüləri qəbul edir | Bəli |
| Kriteriyalar | Inclusion Criteria: 1. Willing and able to provide signed informed consent. 2. Are 18 years or older 3. Have a diagnosis of moderate-to-severe OI based on various clinical features 4. Have genetic mutations that include glycine substitution in COL1A1 or COL1A2, or pathogenic variants in CRTAP, PPIB, or LEPRE1 (if genetic information is unavailable at screening, this may be assessed at screening visit on a clinical or research basis). 5. Females of child-bearing potential must have a negative urine pregnancy test, agree to and have the ability to use acceptable birth control method for entire duration of the study. 6. For Males enrolled in the study, partners must agree to use an acceptable form of birth control for the entire duration of the study. Exclusion Criteria: 1. Fracture less than 3 months prior to the screening visit. 2. Rodding or instruments that prevents reliable bone mineral density (BMD) assessment. 3. Have a known unhealed fracture involving a long bone. 4. Do not meet laboratory safety requirements such as: Vitamin D < 15 ng/dL Serum albumin-corrected calcium levels below 8 mg/dL, Hemoglobin < 10 g/dL, Platelet count < 75,000mm3;, Prothrombin time/(PT/INR) international normalized ratio > 1.5 times Upper Limit of Normal (ULN), Clinical or laboratory abnormality of Grade III or higher as assessed by CTCAE v4.0 which in the view of investigator would compromise safety. 5. Have an EKG with QTc of > 450 ms 6. Have a known allergy to fresolimumab. 7. Have current clinically significant infection. 8. Have a personal history of basal cell carcinoma, squamous cell carcinoma or keratoacanthomas, a personal history of cancer, recent or remote. 9. Have evidence of untreated cavities or planned invasive dental work during the study period. 10. Have had organ transplantation. 11. Have known or suspected valvular heart disease. 12. Plan to have skeletal surgery in the study period. 13. Have had osteotomy 5 months prior to the screening visit. 14. Being treated with zoledronic acid or pamidronate less than 12 months of screening OR oral bisphosphonates less than 6 months of screening OR teriparatide less than one year of screening. 15. Being treated with systemic glucocorticoids 16. Have autoimmune diseases being treated with glucocorticoids or other biologic agents. 17. Enrolled in another clinical trial and receiving treatment with another investigational agent 18. Pregnant or planning to get pregnant during the study period. 19. Nursing mothers. |
Nəticə
İlkin nəticə tədbirləri
1. Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 [6 months for single dose study and 12 months for repeat dose study]
İkincili Nəticə Tədbirləri
1. Percentage change in type 1 procollagen, N-terminal or P1NP, Osteocalcin or Ocn, and C-terminal telopeptide or CTX [6 months in single dose study and 12 months in repeat dose study]
2. Percent change in the areal BMD at the lumbar spine and hip [6 months in single dose study and 12 months in repeat dose study]
3. Difference in score of numeric rating scale for pain [12 months]
4. Change in ml in FEV1 [12 months]
5. Change in ml in FVC [12 months]
6. Percent change in volumetric bone mineral density at the radius [12 months]
7. Number of meters walked in 6 minutes [12 months]
