Drug Database
KD

KD2-305 (KD2305 / KD 2305)

✓ Approved

Meiji Holdings · Recombinant Proteins · Recombinant Proteins

What is KD2-305?

KD2-305 is a recombinant proteins developed by Meiji Holdings. It is approved for therapeutic indications via unknown.

Drug Profile

Brand NamesKD2305, KD 2305
CompanyMeiji Holdings
Drug ClassRecombinant Proteins
RouteUnknown
StatusApproved

Therapeutic Indications

KD2-305 is developed for 2 unique indications across 1 therapeutic area.

Therapeutic AreaConditionPhase
Congenital, familial and genetic disordersFactor IX deficiency✓ Approved
Congenital, familial and genetic disordersFactor VIII deficiency✓ Approved

Related Research Articles

PubMedNew Zealand veterinary journal2026-08-30

Congenital musculoskeletal disease associated with selenium deficiency in calves in Argentina.

Plaza F F, Sosa E E, Ambrosino A A, Poo J J et al.

On two occasions, increased perinatal losses were reported in two beef cattle herds under extensive rearing conditions in Buenos Aires province, Argentina, during the winter calving season of 2025. Affected calves were born weak, unable to stand and suckle, and died within 1-3 days of birth. Cumulative incidences of 10% (33/330) and 3.9% (12/305) were recorded, with 100% case fatality. Necropsies were performed on three calves: two from Outbreak 1 (one calf died within 1 day of birth and one within 3 days) and one calf that died within 1 day of birth from Outbreak 2. Grossly, in all three calves, pelvic limbs and sublumbar muscles exhibited multifocal-to-coalescent pale whitish discolouration, interspersed with haemorrhage. Microscopically, skeletal muscles presented polyphasic degeneration and necrosis of myofibres with calcified deposits within the sarcoplasm. Low Se concentrations (<0.75 mg/kg) were detected in the livers of all three calves, while Cu and Zn concentrations were within reference ranges. No evidence for the involvement of infectious agents was detected. Low Se concentrations were observed in serum samples from 18 dams from Outbreak 1 and nine from Outbreak 2. Mineral analysis of available feed from both farms showed low Cu concentrations in both outbreaks and elevated S concentrations in Outbreak 2. Nutritional myopathy (NM) in beef calves, presumed to be associated with Se deficiency in calves born to Se-deficient dams. Se deficiency was the most likely cause of NM, but high dietary SO4-2 and S concentration in Outbreak 2 may have interfered with dietary Se absorption. Our study highlights that NM should be considered as a potential cause of perinatal losses.

PubMedArchives animal breeding2026-08-29

Genetic analysis of DDR1 polymorphisms as robust markers for milk yield in Simmental cattle.

Şengül Gülüzar G, Özdemir Memiş M

This study aimed to determine new polymorphisms in 15 exon regions of the discoidin domain receptor tyrosine kinase 1 (DDR1) gene. A total of 72 Simmental cattle were used in this study. Single nucleotide polymorphisms (SNPs) of gene regions were performed using polymerase chain reaction (PCR) high-resolution melting (HRM) analysis followed by sequence analysis. The identified DDR1 gene regions include the g.28183947 G/T polymorphic region for the 1' exon region of the DDR1 gene, g.28183480 G/C and g.28183434 C/A-G polymorphic regions for the 3' exon region of the DDR1 gene, g.28181525 C/A polymorphic region for the 5' exon region of the DDR1 gene, g.28180846 G/C polymorphic region for the 6' exon region of the DDR1 gene, g.28180437 C/G polymorphic region for the 7' exon region of the DDR1 gene, g.28178065 G/C polymorphic region for the 10' exon region of the DDR1 gene, g.28175989 G/T polymorphic region for the 12' exon region of the DDR1 gene and g.28173956 T/G and g.28173954 T/C polymorphic regions for the 16' exon region of the DDR1 gene. As a result of the statistical analysis, a significant relationship was found between the g.28183947 G/T polymorphic region in the 1' exon region of the DDR1 gene and the 305 d milk yield ( P < 0.05 ). A significant relationship was found between the g.28181525 C/A polymorphic region in the 5' exon region of the DDR1 gene and daily average milk yields, lactation milk yields and the 305 d milk yield ( P < 0.05 ). No significant relationship was found between the other polymorphic regions detected and milk yields ( P > 0.05 ). Consequently, the genotype and allele gene frequencies of the detected new polymorphic regions were determined. This study suggests that DDR1 gene polymorphic regions found to affect milk yield in Simmental cattle can be used as new candidate molecular markers in animal breeding and selection.

PubMedJournal of hazardous materials2026-08-29

Immobilization of fungal cells on positively charged cyclodextrin-based carriers: Enhanced PhAC degradation and multi-omics implications.

Tu Yizhou Y, Wu Yizhou Y, Pan Yang Y, Ding Xiaolu X et al.

The rational design of cellular interfaces is essential for advancing biocatalytic systems. White rot fungi are promising biodegraders of pharmaceutically active compounds (PhACs), but they are readily inactivated in wastewater treatment, while conventional carriers cannot simultaneously immobilize cells and retain extracellular enzymes. In this study, a stable fungus-enzyme synergistic interface was constructed by assembling Trametes versicolor with a positively charged porous thienyl cyclodextrin polymer (Th-CDP) to form Tv@Th-CDP. This design simultaneously immobilized fungal cells and retained their secreted laccases within the carrier, enhancing PhAC removal in continuous-flow reactors treating secondary municipal effluent to 93%. The system demonstrated sustained 30-d performance and reduced effluent toxicity by 58%. This performance was associated with the high positive charge density of Th-CDP, which enhanced mycelial attachment and laccase retention (48.2 U kg-1). Furthermore, the hydrophobic cavities of cyclodextrin, coupled with electrostatic interactions, enhanced PhAC adsorption and enriched Trametes sp. (46%). This immobilization strategy improved the fungus-enzyme interactions, with enhanced laccase-related catalytic currents observed in electrochemical assays. Metaproteomics analysis and transformation pathway identification supported a degradation model mediated by electrostatic interactions between the fungus and the retained enzymes. A total of 305 proteins associated with oxidoreductase activity were enriched, while the key enzymes aldehyde dehydrogenase (ALDH) and epoxide hydrolase (EPHX2) were upregulated. These changes coincided with enhanced C-N bond cleavage, indicating activation of associated metabolic pathways. Overall, this study provides mechanistic understanding of immobilization mediated by electrostatic interactions and demonstrates its potential to improve the biodegradation of emerging contaminants in engineered biocatalytic systems.

PubMedEnvironmental monitoring and assessment2026-08-29

Measurement-driven GIS mapping of short-term outdoor campus noise at Batman University, Türkiye: A WHO-informed screening approach.

Durmus Barbaros B

This study applied a measurement-driven, GIS-supported workflow to screen short-term outdoor noise conditions at the Batı Raman Campus of Batman University, Türkiye. The verified dataset comprised 355 georeferenced LAeq,10-min observations collected at 305 sampling locations over 14 monitoring days between 8 December 2025 and 3 January 2026. Analyses were restricted to the actively used outdoor campus area, defined as the operational human-exposure domain. The workflow integrated IDW interpolation and cross-validation, descriptive time-window comparison, study-defined screening bands contextualized with reference to WHO environmental-noise guidance, and FDR-corrected Getis-Ord Gi* analysis. Observed LAeq,10-min values ranged from 20.00 to 88.58 dB(A), with a mean of 48.88 ± 13.36 dB(A) and a median of 47.98 dB(A). For the selected IDW configuration (p = 2, k = 12), leave-one-out cross-validation showed minimal average bias but only moderate point-level predictive performance (RMSE = 11.79 dB(A), MAE = 8.55 dB(A), ME =  - 0.08 dB(A), and r = 0.52). Differences among the predefined time windows were not statistically significant (p = 0.169). Of all observations, 43.10% were below 45 dB(A), whereas 33.24% were at or above 55 dB(A). The Gi* analysis identified 100 cold-spot and 57 hot-spot locations among 276 coordinate-unique site means, conditional on the specified spatial-weighting configuration. The study provides an empirical decision-support framework for identifying relative spatial patterns and follow-up monitoring priorities. Its findings represent short-term, sample-supported outdoor conditions and should not be interpreted as annual exposure, formal WHO compliance, indoor exposure, or high-precision prediction.

PubMedThe Lancet regional health. Europe2026-08-29

Acute viral bronchiolitis before and after implementation of nirsevimab prophylaxis in Italy: a multicentre retrospective cohort study.

Spatuzzo Mattia M, Corsello Antonio A, Riccò Matteo M, Bonci Enea E et al.

Acute viral bronchiolitis is the leading cause of hospitalisation in the first year of life, with Respiratory Syncytial Virus (RSV) accounting for more than 60% of cases. A long-acting monoclonal antibody (nirsevimab) has been introduced for infants entering their first epidemic season. 2024-2025 season was the first with nirsevimab availability in Italy. We assessed its impact on bronchiolitis-related utilisation and clinical and virological characteristics of hospitalised infants. We conducted a multicentre retrospective cohort study including infants <12 months with all-cause bronchiolitis during two seasons: pre-implementation (October 2023-April 2024) and post-implementation (October 2024-April 2025). Data were collected from 30 university hospitals across 15 regions using ICD-10 codes. Outcomes were compared using propensity score matching and multivariate regression analyses. Following implementation, emergency department visits decreased by 48% (5076 vs 2633), pediatric ward admissions by 48% (2734 vs 1473) and pediatric intensive care unit admissions by 61% (334 vs 131). Analyses adjusted for local rollout showed reductions of 82% (RR 0.18), 84% (RR 0.16) and 79% (RR 0.20), respectively. Post-implementation, infants were older (aOR 1.07, 95% CI 1.04-1.10) with lower odds for low- (aOR 0.67, 95% CI 0.55-0.82) and high-flow (aOR 0.8; 95% CI 0.65-0.99) oxygen-therapy. RSV remained predominant (934/1473, 63%), while non-RSV infections increased (334/2734, 12% vs 305/1473, 21%). Most infants had not received prophylaxis; 372 (25%) hospitalised despite nirsevimab were younger (5.2 ± 3.5 vs 2.8 ± 1.9, p < 0.001) and had more comorbidities (11%, 82/745 vs 22%, 37/168, p < 0.001). In Italy, nirsevimab was associated with reduced all-cause bronchiolitis-related utilisation and milder disease. Underlying conditions remained a determinant for severe outcomes despite prophylaxis. No funding was received for this study.

PubMedJournal of orthopaedic science : official journal of the Japanese Orthopaedic Association2026-08-28

Nationwide evaluation of late diagnosis of developmental dysplasia of the hip and avascular necrosis after treatment: Insights from the JPOA registry.

Nakamura Tomoyuki T, Kitano Toshio T, Seki Atsuhito A, Iba Kousuke K et al.

The Japanese Pediatric Orthopaedic Association (JPOA) established a nationwide registry for pediatric orthopaedic diseases in 2020. National-level data on late-diagnosed developmental dysplasia of the hip (DDH) and avascular necrosis (AVN) after treatment remain limited. This study aimed to evaluate the frequency of the late diagnosis of DDH, estimate the potential impact of the recommended screening/referral criteria, and identify factors associated with AVN using registry data. This retrospective observational study analyzed DDH patients registered between January 2020 and March 2025. A late diagnosis was defined as a diagnosis at ≥12 months of age. Among patients included in the B-registration with complete baseline data, 408 were analyzed for the late diagnosis of DDH. AVN was assessed according to the Salter criteria; 278 patients (305 hips) with available reduction and AVN data were included in the AVN analysis. Multivariable logistic regression was performed to identify independent factors associated with the late diagnosis of DDH and AVN. Late diagnosis occurred in 60 of the 408 patients (14.7%). Referral by an orthopaedic surgeon was independently associated with the late diagnosis of DDH. Among the late-diagnosed patients, 19 (32%) had registry-recorded characteristics that would have met the recommended referral criteria. Under a hypothetical best-case assumption that all 19 patients would have been diagnosed before 12 months of age, the late-diagnosis rate would theoretically have decreased to approximately 10%. AVN occurred in 17 of the 305 hips (5.6%). Relative to Pavlik harness treatment, closed reduction (OR 3.58) and open reduction (OR 11.70) were independently associated with higher odds of AVN. The late diagnosis of DDH remains prevalent in Japan. Strengthening the implementation of the recommended screening/referral criteria may reduce delayed diagnoses. AVN was independently associated with the reduction method, underscoring the importance of early detection and appropriate treatment selection to minimize complications.

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