
Preliminary data from an ongoing clinical trial suggest that AVR-RD-04 has been well-tolerated.
Preliminary data from an ongoing clinical trial suggest that AVR-RD-04 has been well-tolerated.
In a mouse model of MPS II, IDS.ApoEII effected completely normalized brain pathology and behavior.
Adverum Biotechnologies’ multicenter, double-masked LUNA trial will enroll 72 patients aged 50 years or older.
A substantial benefit noted for EtranaDez and val-rox is that they are delivered as a single-dose.
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In nonclinical studies, AK-OTOF was well-tolerated in both mice and non-human primates.
The disease models used also helped to establish the function of NPHP5 in cilia morphogenesis.
The announcement comes after positive top-line results in the ongoing KarMMa-3 study.
Improved functional activity compared to ROR-1-targeted CAR-T therapies without the 2 forms of reprogramming was demonstrated in preclinical studies.
Of the 8 treated patients who were evaluable, 6 patients had stable disease at Day 28.
Among the 31 patients evaluable for efficacy analysis, ORR was 100%.
SLN124 was well-tolerated in a previous clinical trial involving healthy volunteers.
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Of 55 evaluable patients in ZUMA-3, 71% achieved complete remission (CR) or CR with incomplete hematological recovery (CRi).
Immusoft plans to begin the phase 1 clinical trial of ISP-001 before the end of 2022.
The study’s primary end points are change in visual acuity and the occurrence of adverse events.
The risk-benefit assessment determined that there are no significant safety concerns.
RGX-121 was well-tolerated across all 3 of the dose cohorts with no treatment-related serious adverse events reported.
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A pre-treatment TME with high levels of cytokines and chemokines was associated with complete response to axi-cel treatment.
In an ovarian cancer mouse model, the combination therapy group showed an 83% increase in survival duration compared to an untreated group.
The study will be carried out in Paris and is expected to begin before the end of the year.
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A case study showed that the patient achieved a complete response in 12 months after treatment with CARsgen Therapeutics’ cell therapy.
Thirty-five patients were previously treated with Innovative Cellular Therapeutics’ GCC19CART in an IRB-approved trial in China.
All patients with NMOSD who received CT103A showed improved Expanded Disability Status Scale scores.
The BLA was supported by data from 2 intrapatient, placebo-controlled clinical trials.
Higher doses were associated with improved overall survival, event-free survival, and relapse-free survival.
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The novel therapy targets a hormone receptor only expressed at immunologically relevant levels in the ovaries.