Примери за използване на Binding antibodies на Английски и техните преводи на Български
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Sixty-two of 2,237(2.8%)patients developed binding antibodies.
Binding antibodies do occur as expected with all biologics;
A total of 3.2%(9/282) subjects had binding antibodies to TPO at any time during romiplostim treatment.
Binding antibodies do occur as expected with all biologics; however, they have not been associated with neutralising activity at present.
In paediatric studies,the incidence of binding antibodies to romiplostim at any time was 7.8%(22/282).
Binding antibodies against impurities such as rFurin, CHO-protein or mouse IgG were not observed after treatment with VEYVONDI.
Denosumab pharmacokinetics were not affected by the formation of binding antibodies to denosumab and were similar in men and women.
The incidence of binding antibodies(excluding predose and transient positive patients) was.
Nineteen of 55 patients(35%) who had received Rilonacept Regeneron for at least 6 weeks tested positive for treatment-emergent binding antibodies on at least one occasion.
The presence of anti-evolocumab binding antibodies did not impact the pharmacokinetic profile, clinical response, or safety of Repatha.
The immunogenicity of YESCARTA has been evaluated using an enzyme-linked immunosorbent assay(ELISA)for the detection of binding antibodies against FMC63, the originating antibody of the anti-CD19 CAR.
Binding antibodies do occur as expected with all biologics; however, they have not been associated with neutralising activity at present.
Anti-volanesorsen antibody formation affecting pharmacokinetics The formation of binding antibodies to volanesorsen appeared to increase total Ctrough by 2- to 19-fold.
Binding antibodies do occur as expected with all biologics; however, they have not been associated with neutralising activity at present.
Using a sensitive immunoassay< 1% of patients treated with denosumab for up to 5 years tested positive for non neutralising binding antibodies with no evidence of altered pharmacokinetics, toxicity, or clinical response.
The incidence of binding antibodies(excluding predose positive patients) was 1% as detected by the acid-dissociation ELISA and< 1% as detected by the Biacore assay;
One of the 80 subjects who received VEYVONDI peri-operatively in clinical studies developed treatment-emergent binding antibodies against VWF following a surgery for whom no adverse events or lack of haemostatic efficacy has been reported.
Treatment of VWD patients who have high-titer binding antibodies(due to previous treatment with pdVWF) may require a higher dose to overcome the binding antibody effect and such patients could be managed clinically by administration of higher doses of vonicog alfa based on the PK data for each individual patient.
Data from 409 subjects participating in several neuroblastoma studies and having samples available for the determination of human anti-chimeric antibodies(HACA) demonstrated that 71(17%)developed binding antibodies and 15(4%) developed a neutralising antibody response.
The patients whose sera tested positive for binding antibodies were further evaluated for neutralising antibodies and none of the patients tested positive for neutralising antibodies. .
The immunogenicity of VEYVONDI was assessed in clinical trials by monitoring the development of neutralizing antibodies against VWF and FVIII,as well as binding antibodies against VWF, Furin, Chinese Hamster Ovary(CHO) protein and mouse IgG.
While 5.8% and3.9% of the subjects were positive for developing binding antibodies to romiplostim and TPO respectively, only 2 subjects(0.4%) were positive for neutralising antibodies to romiplostim but these antibodies did not cross react with endogenous TPO.
So a B cell-- it has its membrane bound antibody, just like that.
Let's say we have a B cell andit's got its membrane bound antibody on it.
The incidence of binding antibody post treatment was 16%(3/19) to romiplostim, of which 5.3%(1/19) were positive for neutralising antibodies to romiplostim.
The assay relies on the competition for binding antibody between drug conjugate and free drug which may be present in the urine specimen being tested.
So all of the membrane bound antibodies, all 10,000 or so of them on this B cell, they all expressed the same variable part.
And so these-- the variable ends of these membrane bound antibodies are specific to certain parts of certain pathogens, to certain epitopes.
Relies on the competition for binding antibody between drug conjugate and free drug which may be present in the urine specimen being tested.
Confirmed adult patients were included in this study; for these patients,the incidence of binding antibody post treatment was 3.8%(7/184) to romiplostim, of which 0.5%(1/184) was positive for neutralising antibodies to romiplostim.