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snake venom antibody-2 (ViperaTAb)

✓ Approved

MicroPharm · Polyclonal Antibodies · Polyclonal Antibodies

What is snake venom antibody-2?

snake venom antibody-2 is a polyclonal antibodies developed by MicroPharm. It is approved for therapeutic indications via injectable (others) or intravenous (iv).

Drug Profile

Brand NamesViperaTAb
CompanyMicroPharm
Drug ClassPolyclonal Antibodies, Antibody
RouteInjectable (Others), Intravenous (IV)
StatusApproved

Therapeutic Indications

snake venom antibody-2 is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Injury, poisoning and procedural complicationsVenom poisoning✓ Approved

Related Research Articles

PubMedKidney international2026-05-24

Effectiveness and mechanistic effects of green mamba peptide MQ232 in an orthologous mouse model of Autosomal Dominant Polycystic Kidney Disease.

Wang Xiaofang X, Jiang Li L, Nanayakkara Kavini K, Sun Xiaobo X et al.

Tolvaptan, a vasopressin V2 receptor (V2R) inverse agonist, is the only treatment specifically approved for Autosomal Dominant Polycystic Kidney Disease (ADPKD). In addition to inhibiting cAMP synthesis, it has other effects on V2R signaling. Our goal was to mechanistically characterize the effects of MQ232, an optimized peptide of the green mamba snake and new V2R inverse agonist, in Pkd1RC/RC mice. Pkd1RC/RC mice were treated with MQ232 (0.5, 2, 4 or 8 nmols/kg/hour via minipump), tolvaptan (0.2% in chow) or vehicle from four to 16 weeks of age. MRI measurements of kidney volume were used for randomization and endpoint, urines collected at 12 and 16 weeks, and mice were sacrificed at 16 weeks for blood and tissue collections. MQ232 and Tolvaptan equally attenuated PKD. In male mice, increasing doses of MQ232 were associated with greater reductions in kidney cAMP, aquaporin-2 expression and phosphorylation, and with higher urine outputs, but equally ameliorated PKD; there was no correlation between kidney cAMP or urine output with disease attenuation. Phosphorylated/total ratios for Src, ERK, CRAF, Akt, RPS6, and Stat3 were in general lower in the treated mice, but this was less or reversed with increasing MQ232 doses. Analysis of previous studies with Tolvaptan showed similar dose dependent effects. This is consistent with these compounds being dual efficacy V2R ligands with inverse agonistic activity on Gαs/cAMP and, at high doses, activating β-arrestin dependent or independent Src and ERK signaling. Both compounds downregulated PAPPA. MQ232 inhibited IGF1Rβ phosphorylation whereas Tolvaptan at the dose/schedule used in the study did not. Vasopressin binding to V2R activates many cystogenic pathways: Gαs/cAMP, β-arrestin-Src and -ERK, and PAPPA and IGF1R signaling. Activation of cAMP-independent signaling may limit the benefit from MQ232 and Tolvaptan when administered at high doses, questioning the rationale of titrating these compounds to maximally tolerated doses to treat ADPKD. Improved understanding of V2R signaling in ADPKD will lead to better therapies.

PubMedFish & shellfish immunology2026-05-24

Preparation and application of IgM monoclonal antibodies in half-smooth tongue sole (Cynoglossus semilaevis).

Qiu Jiamin J, Zhang Jialin J, Qian Xiaorui X, Wu Jiong J et al.

In this study, the native IgM of half-smooth tongue sole (Cynoglossus semilaevis), an economically important marine flatfish, were purified, and used as the immunogen for preparation of monoclonal antibody (mAb). Based on the mAbs, double-antibody sandwich ELISA was constructed for the detection of IgM in C. semilaevis serum and capture ELISA were established for vaccine efficacy evaluation. Results showed that two monoclonal antibodies (mAbs) specifically targeting IgM of half-smooth tongue sole (Cynoglossus semilaevis) were successfully obtained (designated as 3A12 and 5F39). The mAbs exhibited high specificity to native C. semilaevis IgM, without cross-reactivity with IgM from other teleost species. Furthermore, a double-antibody sandwich ELISA was further established for the detection of serum IgM in C. semilaevis with the mAbs pair, which showed a linear detection range of 0.156-10 μg/mL for purified IgM, with a limit of detection (LOD) of 0.313 μg/mL. Using the developed sandwich ELISA, it was found that the IgM level in large-sized fish was significantly higher than that in small-sized fish, and immunostimulants could remarkably enhance the IgM level in fish. Moreover, the specific IgM antibody levels in the serum of C. semilaevis after immunization with inactivated Vibrio vulnificus were analyzed by capture ELISA using mAb 5F39 as the detection antibody, a time-dependent variation trend was found in the specific IgM antibody titer among the immunized group. In conclusion, the mAbs targeting C. semilaevis IgM could specifically and efficiently recognize the native IgM protein, and served as a reliable tool for the detection of serum IgM, providing essential technical support for immune status assessment and vaccine development in C. semilaevis aquaculture.

PubMedCancer science2026-05-24

Tumor-Derived Extracellular Vesicles in Plasma for Predicting Anti-PD-1 Antibody Efficacy in Non-Small Cell Lung Cancer.

Kinoshita Tomonari T, Ohta Shigeki S, Wakui Seiki S, Maeda Chihaya C et al.

Liquid biopsy is a promising biomarker for cancer detection and prediction of therapy responses. In this study, we developed new antibody-based sandwich assays to measure three extracellular vesicle (EV) subsets that express cell surface vimentin (CSV) and co-express epithelial cell adhesion molecule (EpCAM) or PD-L1 in plasma. Fifty-seven non-small cell lung cancer (NSCLC) patients who underwent complete resection and 89 stage IV NSCLC patients who received anti-PD-1 antibody were enrolled. Correlations between the plasma EV subsets at baseline and various clinicopathological factors were evaluated. Plasma EpCAM/CSV-EV levels were significantly higher in stage I NSCLC patients compared to healthy donors, suggesting this may be a valuable biomarker for detecting early-stage NSCLC. High plasma CSV/CSV-EV levels at baseline were significantly correlated with a poor prognosis after treatment, both in the surgery cohort and the anti-PD-1 antibody cohort, which suggests that this may be useful for predicting the post-treatment prognosis in NSCLC patients. High plasma CSV/PD-L1-EV levels at baseline were significantly correlated with poor postoperative prognosis. However, high plasma CSV/PD-L1-EV levels at baseline were significantly correlated with a favorable clinical response and prognosis following anti-PD-1 antibody treatment in stage IV NSCLC. Therefore, plasma CSV-related EV subsets at baseline may be attractive biomarkers for early cancer detection (EpCAM/CSV), prediction of postoperative prognosis (CSV/CSV), and prediction of clinical responses and prognosis after anti-PD-1 antibody therapy (CSV/PD-L1). These EV subsets can be easily measured repetitively at appropriate timing. These novel liquid biopsies may be additional and complementary diagnostic biomarkers for NSCLC patients.

PubMedNeurology and therapy2026-05-24

Safety and Efficacy of Obinutuzumab β (MIL62), a Novel Glycoengineered Type II Anti-CD20 Monoclonal Antibody, in Patients with Neuromyelitis Optica Spectrum Disorder: A Multicenter, Single-Arm, Phase Ib Clinical Trial.

Wu Lei L, Wei Min M, Gao Feng F, Zhang Hua H et al.

To evaluate the safety, pharmacokinetics, pharmacodynamics, and efficacy of obinutuzumab β, a novel glycoengineered type II anti-CD20 monoclonal antibody, in patients with neuromyelitis optica spectrum disorder (NMOSD). In this multicenter, open-label, single-arm, phase Ib trial (NCT05314010), 11 aquaporin protein-4 (AQP4)-IgG-positive patients with NMOSD received obinutuzumab β at 500 mg or 1000 mg on days 1 of weeks 1 and 3. Patients in the 500-mg group could escalate to 1000 mg after 24 weeks if tolerated. Evaluations occurred at specified weeks (24-208), with 1000-mg doses on days 1 of weeks 25, 27, and every 26 weeks thereafter in patients who are relapse-free. Safety, efficacy, pharmacokinetics, pharmacodynamics, and immunogenicity were assessed. All participants with 500 mg (n = 3) transitioned to 1000 mg after 24 weeks. During the entire study period, all 11 participants experienced at least one treatment-emergent adverse event (TEAE); 90.9% had treatment-related adverse events (TRAEs). Serious adverse events were reported in 54.5%, with 27.3% related to obinutuzumab β. No TEAEs or TRAEs led to treatment discontinuation, withdrawal, or death. Two patients had early relapses on days 26 and 27 post-first dose, respectively; one withdrew immediately, while the other remained on treatment for 1 year. The 2-year disease relapse-free rate was 81.8% [95% confidence interval (CI): 44.7%, 95.1%], and the annualized relapse rate (ARR) declined from 1.3 before 2-year treatment to 0.2 (95% CI: 0.1, 0.2) after obinutuzumab β, representing an 87.7% reduction. Obinutuzumab β demonstrated manageable safety and may have promising efficacy against NMOSD. Despite the lack of a comparator group, the results support evaluation in phase III trials. https://clinicaltrials.gov/ (#NCT05314010).

PubMedBMC cancer2026-05-24

High TROP-2 expression as a predictor of poor neoadjuvant chemotherapy response in luminal B breast cancer: a retrospective clinicopathological study.

Öztürk Çiğdem Ç, Çubukçu Safiye Sümeyye SS, Şen Bayram B, Öztürk Ahmet Emin AE et al.

Trophoblast cell surface antigen 2 (TROP-2) is a type I transmembrane glycoprotein that is expressed on the cell surface. It is overexpressed in various epithelial malignancies. Due to its protumoral biological effects and its role as a target receptor for antibody-drug conjugates, TROP-2 is of particular clinical interest. This study aims to investigate the relationships between TROP-2 expression, clinicopathological parameters, and response to neoadjuvant chemotherapy in invasive breast carcinomas. TROP-2 expression was evaluated by immunohistochemically from 211 cases of invasive breast carcinoma. The H-score was used in the TROP-2 assessment. Cases with a score of 0-200 were considered low, and cases with a score above 200 were considered high TROP-2 expression. High TROP-2 expression was significantly associated with HER2 negativity (p = 0.019), lymph node metastasis (p = 0.016), and a poor response to neoadjuvant chemotherapy (RCB-II/III) (p = 0.01). Multivariate analysis revealed that molecular subtype, stromal tumor-infiltrating lymphocytes, and high TROP-2 expression were independent predictors of neoadjuvant chemotherapy response. High TROP-2 expression was found to be associated with adverse clinicopathological parameters and poor response to neoadjuvant chemotherapy, and was identified as an independent predictive biomarker for neoadjuvant response. The lower pathological complete response rates observed in luminal B molecular subtype breast carcinomas with high TROP-2 expression suggest that TROP-2-targeting agents should be investigated more thoroughly in the neoadjuvant therapy setting, particularly in LB subtype cases. Furthermore, assessing TROP-2 expression in each case will aid in optimal patient selection for treatment and contribute to the personalization of oncological therapy.

PubMedVeterinary research communications2026-05-24

Genetic evolution analysis and clinical antibody tracking analysis of two PEDV strains in China.

Jiang Lei L, Wang Lei L, Zhao Ying Y, Fan Jinghui J et al.

To investigate the current epidemic status of dominant Porcine Epidemic Diarrhea Virus (PEDV) strains and the genetic evolution characteristics of their S proteins in China, as well as to explore strategies for enabling suckling piglets in PED-affected farms to acquire effective maternal antibody protection, this study conducted S gene sequencing on PEDV isolates collected from two epidemic cases, followed by phylogenetic analysis and homology-based three-dimensional modeling. Meanwhile, the titers of IgA and IgG in the PEDV-specific immune response were tracked and analyzed by employing different immunization regimens. The results showed that phylogenetic analysis allowed the identification of distinct variations in the major antigenic epitope CO-26 K equivalent (COE) region and the predicted N-glycosylation sites of the S protein. Additionally, the differences in the spatial conformation of the COE region might also account for the inadequate protection of pig herds against G2c strain infection conferred by commercial vaccines that do not contain the G2c strain. Furthermore, feedback immunization combined with inactivated tissue vaccine-based sow booster immunization during gestation could induce high levels of PEDV-specific IgA antibodies, and continuous gestation-stage booster immunization with inactivated tissue vaccines was crucial for maintaining such high antibody titers. Collectively, the findings of this study provide a reference for the establishment of high-level PED maternal antibody protection in pig herds.

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