Drug Database
QL

QL-1209 (QL1209 / QL 1209)

✓ Approved

Qilu Pharmaceutical · ERBB2 · 单克隆抗体

什么是 QL-1209?

QL-1209 是一种单克隆抗体,由Qilu Pharmaceutical研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intravenous (IV)。

药物档案

商品名QL1209, QL 1209
公司Qilu Pharmaceutical
药物类别单克隆抗体, 抗体
分子靶点ERBB2
给药途径Injectable (Others), Intravenous (IV)
状态Approved

作用机制

分子靶点

QL-1209 作用于 1 个分子靶点:

ERBB2erb-b2 receptor tyrosine kinase 2 (NEU, CD340)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

QL-1209 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Neoplasms benign, malignant and unspecified (incl cysts and polyps)Breast cancer✓ Approved

相关研究文献

PubMedmedRxiv : the preprint server for health sciences2026-10-25

LLM-assisted evidence audit of late-stage cancer incidence as a screening trial endpoint.

Li Shiyin S, Zhang Wanheng W, Xing Xing X, Shen Ziyuan Z et al.

Late-stage cancer incidence is being considered as an earlier endpoint in cancer-screening trials, but its trial-level association with cancer-specific mortality may depend on evidence selection and endpoint harmonization. We evaluated the robustness of this association to source-verified additions. We reconstructed the PubMed corpus underlying a 41-comparison review. Gemini 3.1 Pro Preview was used only to prioritize reports for blinded human reassessment. Reviewers determined eligibility, linked reports from the same trial, harmonized endpoints, and verified comparison-level data. We recalculated unweighted Pearson correlations overall and by cancer type after adding earliest-compatible trial comparisons. Among 1209 candidate records, 996 PDFs were assessed. Thirty-three reports absent from the source review were prioritized; 26 were eligible, representing 18 trials, and 8 provided compatible comparisons. Adding these comparisons increased the dataset from 41 to 49 and attenuated the overall correlation from 0.73 (95% confidence interval [CI] = 0.55 to 0.85) to 0.59 (95% CI = 0.37 to 0.75). Updated correlations were 0.49 (95% CI = -0.26 to 0.87) for breast, - 0.23 (95% CI = -0.71 to 0.40) for colorectal, and 0.83 (95% CI = 0.54 to 0.95) for lung cancer. One sparse-event comparison influenced the colorectal estimate. The overall association was sensitive to evidence composition, and cancer-specific stability varied. Late-stage incidence should be evaluated by cancer type and with prespecified sensitivity analyses for evidence selection and endpoint definitions. Model-assisted prioritization cannot replace human eligibility review, trial reconciliation, and source verification.

PMID 42922838
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PubMedInternational urology and nephrology2026-10-25

The EMS Swiss LithoClast® Trilogy for the treatment of large bladder stones: a prospective international multicenter study.

Okour Radwan Al RA, Emehute John-Daniel JD, Gupta Mantu M, Gupta Kavita K et al.

The best treatment for large bladder stones remains debated. The options range from open cystolithotomy to minimally invasive endoscopic techniques, including the Mauermayer stone punch and high-power laser cystolitholapaxy, and more recently the EMS Swiss LithoClast® Trilogy, which combines ultrasonic and ballistic energy with continuous suction in a single probe and is well established in percutaneous nephrolithotomy (PCNL). We report the first prospective international multicenter experience of the Trilogy system for the transurethral treatment of large bladder stones. Consecutive patients undergoing cystolitholapaxy with the Trilogy system were enrolled prospectively at five recruiting centers in five countries between August 2023 and December 2024. Procedures were performed transurethrally through rigid sheaths of 20.8 to 26 Fr. The primary outcome was lithotripsy efficiency (preoperative CT-derived stone volume divided by probe activation time). Secondary outcomes were the stone-free rate, device safety and reliability, intraoperative urothelial trauma, postoperative complications, and surgeon-rated ergonomics and efficiency. Outcomes are reported both by intention to treat, in which patients converted to laser are counted as failures, and per protocol, restricted to procedures completed with the Trilogy system alone. Forty-four patients were enrolled (median age 76 years, range 27 to 88). Forty-three procedures were attempted; one could not proceed because of a urethral stricture. The stone could not be fragmented in two patients (4.7%), both dense calculi (1591 HU and 1280 HU), and both were converted to high-power laser, leaving 41 procedures completed with the Trilogy system alone (35 male, 85.4%). By intention to treat, the stone-free rate was 93.0% (40 of 43 attempted procedures) and 90.9% (40 of 44 patients enrolled); the per-protocol rate was 97.6% (40 of 41). Median total stone volume was 5987 mm3 (range 1209 to 66,743) and median stone density was 871 HU (range 75 to 1666). Probe activation time was recorded in an analyzable form in 34 of 41 patients (83%), with a median of 20 min and a median lithotripsy efficiency of 351 mm3/min (interquartile range 215 to 549); median total operative time was 59 min (n = 37). Superficial mucosal injury occurred in 15 patients (37%) and detrusor injury in one (2%); there were no perforations. Two probes broke and two handpieces overheated, but the affected procedures were completed; there were no suction failures. Median surgeon ergonomic and efficiency scores were 7 and 8 out of 10. Complications were minor (two urinary tract infections, Clavien-Dindo II); one unrelated death occurred within 30 days. Where length of stay was recorded (31 of 41 patients), the median was 0 days, with 52% discharged on the day of surgery. Across five international centers, the Swiss LithoClast® Trilogy proved a safe, reliable, and efficient tool for the transurethral treatment of large bladder stones, with high stone-free rates and favorable surgeon feedback. Very dense stones resisted fragmentation in two patients, so extreme stone density remains a technical limitation of the device by comparison with high-power lasers, and the sheath caliber required is large, though similar to that used with laser cystolitholapaxy. Within those limits, and because it is available in centers where PCNL is performed and needs no dedicated laser infrastructure, the Trilogy system is an attractive alternative to high-power lasers, particularly where laser access is limited.

PMID 42927578
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PubMedFood research international (Ottawa, Ont.)2026-10-23

Bioprospecting hidden yeasts in artisanal dairies: Revealing potential probiotics for functional fresh cheese.

Agarbati Alice A, Canonico Laura L, Ciani Maurizio M, Comitini Francesca F

Artisanal dairies represent a significant reservoir of microbial biodiversity, offering unique opportunities to discover novel strains with functional properties. This study aimed to isolate and characterize wild yeast strains from traditional sheep cheese production in Central Italy evaluating their probiotic potential and technological suitability for fresh cheese manufacturing. Twenty-five wild yeast strains, belonging to Candida friedrichii, Candida zeylanoydes, Debaryomyces hansenii, Metschnikowia spp., Kluyveromyces lactis, and Yarrowia lipolytica, were screened for technological traits, including survival in milk, acidification activity, lactose consumption, and salt tolerance. Results identified four promising strains-C. zeylanoydes DiSVA 1132, D. hansenii DiSVA 1156, Metschnikowia spp. F14, and K. lactis DiSVA 1209-which demonstrated high viability under the tested milk-incubation conditions, reaching more than 106-107 CFU/mL in line with the commonly discussed target levels for potential probiotic foods, and significant acidifying capacity (pH reduction to ∼4.5). These strains were used as a microbial consortium in co-fermentation with a commercial Lactobacillus casei strain to produce a functional fresh cheese, following the Squacquerone di Romagna DOP specifications. The yeast pool did not negatively affect the growth of the bacterial starter and significantly enhanced sensory characteristics and preliminary functional-food potential. Sensory analysis confirmed that the yeast consortium improved the perception of texture, consistency, and overall aroma of the final product. These findings highlight the potential of using autochthonous "next-generation" probiotic yeasts to develop innovative functional dairy products with enhanced sensory and technological suitability properties.

PMID 42914242
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PubMedDiabetes, metabolic syndrome and obesity : targets and therapy2026-10-18

Meta-Analysis of the Impact of Low Glycemic Index Dietary Patterns on Blood Glucose Levels and Pregnancy Outcomes in Gestational Diabetes Mellitus.

Zhang Yu Y, Gong Zhiyong Z, Yu Minda M, Gao Ying Y

This systematic review and meta-analysis aimed to evaluate the efficacy of low glycemic index (LGI) dietary patterns in improving glycemic control and pregnancy outcomes among patients with gestational diabetes mellitus (GDM). Randomized controlled trials (RCTs) were identified through systematic searches of PubMed, The Cochrane Library, Web of Science, CNKI, VIP Medicine, Wanfang, and other relevant databases. Data extraction and quality assessment were conducted following Cochrane guidelines. Meta-analyses were performed using RevMan 5.3 and STATA 12.0 software. Eleven RCTs comprising 1209 participants were included. Compared with conventional diabetic diets, LGI dietary interventions significantly reduced fasting blood glucose, 2-hour postprandial blood glucose, glycated hemoglobin (HbA1c), and insulin resistance levels. Additionally, LGI diets were associated with a lower incidence of excessive gestational weight gain and improved neonatal outcomes. LGI dietary patterns effectively enhance glycemic control, mitigate insulin resistance, and improve perinatal outcomes in GDM patients. However, further high-quality studies with larger sample sizes are warranted to strengthen these conclusions.

PMID 42893071
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PubMedPloS one2026-10-15

Expert consensus on the availability and consumption of herbal medicinal products in Thai pharmacies: An e-Delphi study.

Nakaphan Thanat T, Teerachaisakul Monthaka M, Chaotham Chatchai C, Pongpirul Krit K

Despite the growing use of herbal medicinal products (HMPs) in Thailand, factors relevant to their availability and consumption in pharmacies remain insufficiently characterized. Pharmacies and healthcare professionals may play important roles in improving the availability and promoting their appropriate use. A three-round e-Delphi study was conducted among 30 multidisciplinary experts to identify and establish consensus on factors considered relevant to the availability and consumption of HMPs in pharmacies across Thailand. Experts rated the relevance and impact of each factor using a 7-point Likert scale. Consensus was defined as a Quality of the Lower Approximation (QL) score ≥ 0.75. Of the 34 factors assessed, 25 reached consensus across four domains: (1) herbal medicinal products, (2) product information, (3) professional responsibilities, and (4) pharmacy operations. The National List of Essential Herbal Drugs received the highest consensus score (QL = 1.00). All nine product information factors reached consensus. Professional factors reaching consensus included product recommendation, knowledge of HMP categories, and knowledge of evidence-based efficacy and safety. Pharmacy-related factors reaching consensus included pharmacy type, business model, participation in national health programs, and location. Expert consensus identified a set of factors considered relevant to HMP availability and consumption in Thai pharmacies. These findings provided a framework for future empirical studies and may inform policies and interventions related to product information, professional competency, and pharmacy operations.

PMID 42879419
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PubMedSpinal cord2026-10-12

Characterizing ambulation potential following acute traumatic spinal cord injury: a populational cohort study on 1209 patients.

Dionne Antoine A, Richard-Denis Andréane A, Pelletier-Roy Rémi R, Phan Philippe P et al.

Population cohort study. Propose a new paradigm of using a descriptive approach - rather than a predictive tool - to estimate the ambulation potential after traumatic spinal cord injury (TSCI). 30 trauma and rehabilitation centers across Canada participating in the Rick Hansen SCI Registry. A retrospective study of 1209 patients from the Rick Hansen Spinal Cord Injury Registry was conducted. The outcome was the level of outdoor walking 12 months following the SCI: dependent vs. limited vs. independent community ambulators. The actual ambulation outcomes were stratified by AIS severity grade, and by main phenotypes of individuals sharing similar baseline characteristics determined by classification tree analysis. The proportion of participants achieving dependent, limited and independent community ambulation were respectively 94, 4.7 and 1.6% for AIS grade A SCI; 72, 16 and 12% for AIS grade B; 50, 23 and 28% for AIS grade C; and 11, 24 and 65% for AIS grade D. In addition to AIS grade, main phenotypes for ambulation outcomes were associated with lower extremity motor score (LEMS) and mechanism of injury for AIS grade B SCI, as well as LEMS and age for AIS grade C and D SCI. This study proposes a paradigm shift to describe rather than predict ambulation outcomes after TSCI, using a descriptive chart characterizing the potential for recovering community ambulation based on real outcomes observed in the general TSCI population, in order to facilitate estimating the ambulation potential early after TSCI.

PMID 42860442
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