Pharmacokinetics in children
The following kinetic parameters have been observed after administering 10 mg/kg abatacept (to children aged 6-17 years, avg. 40 kg):
Cl: 0.4 ml/hour/kg,
Vd: 0.12 l/kg,
t½: 11.4 days.
dose recommendation of formulary compared to licensed use (on-label versus off-label)
No information is present at this moment.
Available formulations
No information is present at this moment.
Dosages
| Juvenile idiopathic arthritis (JIA) |
- Intravenous
-
2 years
up to
6 years
- Initial dose:
10
mg/kg/dose
once every 2 weeks.
in weeks 0, 2 and 4.
- Maintenance dose:
10
mg/kg/dose
once every 4 weeks.
- Directions for administration:
Administer as an intravenous infusion over 30 minutes
There is no evidence regarding the use of abatacept for JIA in children aged < 6 years. Treatment by or after consultations with a paediatric specialist (rheumatologist) who has experience using abatacept for this indication.
-
6 years
up to
18 years
and
<
75 kg
- Subcutaneous
-
≥ 2 years
and
10
up to
25 kg
-
≥ 2 years
and
25
up to
50 kg
-
87.5
mg/dose
once a week.
-
≥ 2 years
and
≥ 50 kg
|
| Therapy-resistant focal segmental glomerulosclerosis (FSGS) |
- Intravenous
-
6 years
up to
18 years
and
75
up to
100 kg
-
750
mg/dose,
once only.
Multiple doses can be given if necessary; give the first 3 doses every second week and thereafter every four weeks..
- Directions for administration:
Administer as an intravenous infusion over 30 minutes.
There is little evidence regarding the use of abatacept in children with FSGS. Treatment by or after consultations with a paediatric specialist (nephrologist) who has experience using abatacept for this indication.
-
6 years
up to
18 years
and
≥ 100 kg
-
1.000
mg/dose,
once only.
Multiple doses can be given if necessary; give the first 3 doses every second week and thereafter every four weeks.
- Directions for administration:
Administer as an intravenous infusion over 30 minutes.
There is little evidence regarding the use of abatacept in children with FSGS. Treatment by or after consultations with a paediatric specialist (nephrologist) who has experience using abatacept for this indication.
-
2 years
up to
18 years
and
<
75 kg
-
10
mg/kg/dose,
once only.
Multiple doses can be given if necessary; give the first 3 doses every second week and thereafter every four weeks.
- Directions for administration:
Administer as an intravenous infusion over 30 minutes.
There is little evidence regarding the use of abatacept in children with FSGS. Treatment by or after consultations with a paediatric specialist (nephrologist) who has experience using abatacept for this indication.
-
6 years
up to
18 years
and
75
up to
100 kg
[3]
-
750
mg/dose,
once only.
Multiple doses can be given if necessary; give the first 3 doses every second week and thereafter every four weeks..
- Directions for administration:
Administer as an intravenous infusion over 30 minutes.
There is little evidence regarding the use of abatacept in children with FSGS. Treatment by or after consultations with a paediatric specialist (nephrologist) who has experience using abatacept for this indication.
-
6 years
up to
18 years
and
≥ 100 kg
[3]
-
1.000
mg/dose,
once only.
Multiple doses can be given if necessary; give the first 3 doses every second week and thereafter every four weeks.
- Directions for administration:
Administer as an intravenous infusion over 30 minutes.
There is little evidence regarding the use of abatacept in children with FSGS. Treatment by or after consultations with a paediatric specialist (nephrologist) who has experience using abatacept for this indication.
|
Renal impaiment in children > 3 months
GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects in children
Common: infection of the upper respiratory tract (including sinusitis, nasopharyngitis and rhinitis), middle and external ear inflammation, haematuria, pyrexia.
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Warnings & precautions
No information available on specific warnings and precautions in children.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
IMMUNOSUPPRESSANTS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Selective immunosuppressants |
|
|
|
L04AA32
|
|
|
|
L04AA13
|
|
|
|
L04AA02
|
|
|
|
L04AA06
|
|
|
|
L04AA31
|
|
|
|
L04AA04
|
|
|
|
L04AA44
|
| Other immunosuppressants |
|
|
|
L04AX01
|
|
|
|
L04AX03
|
| Tumor necrosis factor alpha (TNF-alpha) inhibitors |
|
|
|
L04AB04
|
|
|
|
L04AB01
|
|
|
|
L04AB06
|
|
|
|
L04AB02
|
| Interleukin inhibitors |
|
|
|
L04AC03
|
|
|
|
L04AC02
|
|
|
|
L04AC08
|
|
|
|
L04AC13
|
|
|
|
L04AC19
|
|
|
|
L04AC10
|
|
|
|
L04AC22
|
|
|
|
L04AC07
|
|
|
|
L04AC05
|
| Calcineurin inhibitors |
|
|
|
L04AD01
|
|
|
|
L04AD02
|
| Sphingosine-1-phosphate (S1P) receptor modulators |
|
|
|
L04AE01
|
| Janus-associated kinase (JAK) inhibitors |
|
|
|
L04AF02
|
|
|
|
L04AF02
|
|
|
|
L04AF08
|
|
|
|
L04AF01
|
| Monoclonal antibodies |
|
|
|
L04AG04
|
| Mammalian target of rapamycin (mTOR) kinase inhibitors |
|
|
|
L04AH02
|
|
|
|
L04AH01
|
| Complement inhibitors |
|
|
|
L04AJ01
|
|
|
|
L04AJ02
|
| Dihydroorotate dehydrogenase (DHODH) inhibitors |
|
|
|
L04AK02
|
References
-
Bristol-Myers Squibb Pharma EEIG, SPC Orencia (EU/1/07/389/001->003) 21-5-2012, www.geneesmiddeleninformatiebank.nl
-
A van Royen., Expert opinie sectie kinderreumatologie JIA 2-6 jaar., 9 april 2015
-
Yu CC et al., Abatacept in B7-1-positive proteinuric kidney disease., N Engl J Med., 2013, 19;369(25), 2416-23
Therapeutic Drug Monitoring
Overdose