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adenovirus vaccines

✓ Approved

Teva Pharmaceutical Industries Ltd. · Vaccine · Vaccine

What is adenovirus vaccines?

adenovirus vaccines is a vaccine developed by Teva Pharmaceutical Industries Ltd.. It is approved for therapeutic indications via oral (po).

Drug Profile

CompanyTeva Pharmaceutical Industries Ltd.
Drug ClassVaccine, Large Molecules
RouteOral (PO)
StatusApproved

Therapeutic Indications

adenovirus vaccines is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Infections and infestationsAdenovirus infection✓ Approved

Related Research Articles

PubMedMedScience2026-09-19

Neoantigen cancer vaccines for gastrointestinal tumors: opportunities and challenges.

Zhao Zixuan Z, Du Xinyu X, Gao Xiaoliang X, Zhao Sheng S et al.

Gastrointestinal tumors are characterized by high global incidence and mortality rates. Although immune checkpoint inhibitors (ICIs) have achieved breakthroughs in some of these cancers, their overall response rate remains low. Neoantigen cancer vaccines have emerged as a promising new strategy for immunotherapy in gastrointestinal tumors due to their high specificity and strong immunogenicity. These vaccines effectively activate specific T-cell immunity and can produce synergistic effects when combined with ICIs. Various vaccine platforms offer distinct advantages, and clinical trials have shown encouraging potential in inducing immune responses and extending progression-free survival. Meanwhile, current challenges and future directions cannot be ignored. Key challenges primarily involve the accuracy of neoantigen prediction, tumor heterogeneity, and optimal treatment timing. Future directions include artificial intelligence (AI)-assisted multi-omics screening, the development of universal vaccines, optimization of novel delivery systems, and multimodal combination strategies. These advances are expected to promote the application of neoantigen cancer vaccines in postoperative recurrence prevention and early-stage treatment, ultimately moving toward personalized precision immunotherapy. This article systematically reviews the clinical progress and prospects of neoantigen cancer vaccines in treating gastrointestinal tumors, aiming to provide insights for immunotherapy in this field and offer new perspectives for further optimization of such vaccines.

PubMedAAPS PharmSciTech2026-09-19

Comprehensive Stability Assessment of Squalene in a Nanoemulsion Adjuvant and the SpiN-Tec Vaccine: HPLC Quantification, Stress Testing, and Stability Studies.

Gomes Isabela Pereira IP, Rivelli Graziella Gomes GG, Bagno Flávia Fonseca FF, Hojo-Souza Natália Satchiko NS et al.

Squalene-based nanoemulsions are widely used as adjuvants in vaccine formulations, but their stability can be affected by environmental factors such as pH, oxidative stress, temperature, and light. We have produced a squalene nanoemulsion (CTVad1) to support the clinical development of new vaccines. This study aimed to develop and validate an HPLC method for squalene quantification in SpiN-Tec, a recombinant protein vaccine against COVID-19. We also aimed to evaluate the stability of the CTVad1 adjuvant and SpiN-Tec under controlled storage conditions. A reversed-phase HPLC method was developed and validated, and comprehensive forced degradation studies were performed on the raw material and SpiN-Tec under acidic, basic, oxidative, thermal, and photolytic conditions to demonstrate the stability-indicating capability of the method. Physicochemical, morphological, and biological characteristics were assessed, and stability studies of both the vaccine and the CTVad1 adjuvant were performed under accelerated and long-term conditions. The HPLC method was selective, precise, accurate, linear, and robust. Squalene raw material degraded under all tested conditions, whereas formulation in nano-sized globules improved its stability, with degradation observed only under hydrogen peroxide and light exposure. CTVad1 remained stable over time, exhibiting only minor, non-critical changes within the specification limits in both accelerated and long-term stability studies, regardless of the glass packaging used (clear or amber). In addition, the SpiN-Tec vaccine maintained its physicochemical and biological integrity under all tested conditions, with all evaluated parameters remaining within the established specification ranges. Our findings demonstrate that proper formulation, packaging, and storage conditions can preserve squalene stability in nanoemulsion-based vaccines, ensuring the quality, safety, and efficacy of the SpiN-Tec vaccine and its adjuvant throughout shelf life.

PubMedEuropean journal of pediatrics2026-09-19

Safety profiles of calcineurin inhibitor-related infections in the pediatric population: a real-world pharmacovigilance analysis.

Lu Yun Y, Zhou Yan Y, Wu Yu Y, Liu Chun C et al.

This study aimed to assess infection-related adverse events (AEs) associated with calcineurin inhibitors (CNIs), including cyclosporine (CsA) and tacrolimus (TAC), in the pediatric population using combined postmarketing surveillance databases. Data from the FDA Adverse Event Reporting System (FAERS) and the Japanese Adverse Drug Event Report (JADER) were analyzed for pediatric patients. Disproportionality analysis was conducted to evaluate AEs. Additionally, subgroup analysis, fatal outcome assessment, and time-to-onset (TTO) analysis were also performed. A total of 426 CsA-related and 1284 TAC-related infection reports were identified in FAERS, with corresponding findings in JADER (CsA, n = 140; TAC, n = 323). Cross-database analysis identified positive overlapping signals for BK virus, cytomegalovirus, and Epstein-Barr virus infections for both drugs. Age- and sex-stratified analysis revealed differences in infection-related reporting patterns, with the percentage of fatal outcomes varying significantly across age groups and being highest in the youngest subgroups: 3-5 years for CsA (29.2%) and 0-2 years for TAC (18.4%) (P < 0.05). This study provides real-world evidence on infection-related safety signals associated with CNIs in pediatric patients, particularly for viral infections. The distinct signal profiles and age- and sex-specific patterns highlight the importance of individualized infection risk monitoring and immunosuppressive management strategies. • Calcineurin inhibitors (CNIs), including cyclosporine (CsA) and tacrolimus (TAC), are widely used in pediatric transplantation and immune-mediated diseases, but infection remains an important safety concern during CNI-based immunosuppression. • Evidence on the comparative infection-related safety profiles of these two agents in children remains limited. • This is the first dual-database pharmacovigilance analysis to characterize infection-related safety signals associated with CsA and TAC in pediatric patients. • Age- and sex-specific patterns were identified, with fatal outcomes significantly associated with younger age groups for both drugs.

PubMedInfectious diseases of poverty2026-09-19

Territorial inequities in access to essential medicines for neglected tropical diseases in a decentralised European health system: a nationwide assessment in Spain.

Belhassen-García Moncef M, de la Calle-Prieto Fernando F, Del Moral Sánchez José Manuel JM, Alonso-Sardón Montserrat M et al.

Neglected tropical diseases (NTDs) represent an increasing but often overlooked challenge for European health systems owing to international mobility, migration, travel, and climate-related changes in disease ecology. Although effective treatments exist for most NTDs and many are included in the World Health Organization (WHO) Model List of Essential Medicines, their availability in decentralised high-income health systems remains poorly characterised. This study assessed the availability, accessibility, and territorial variability of essential medicines for NTDs across the autonomous communities of Spain and identified the main barriers to equitable access. A nationwide, cross-sectional study was conducted across the 17 autonomous communities of Spain. Data were collected between January and December 2025 through a structured survey of Hospital Pharmacy Services in centres with expertise in tropical medicine and infectious diseases and were complemented by expert clinical validation. Medicines were classified according to commercial status, access pathways, dispensing circuits, and regional availability. Descriptive analyses summarised inter-regional variability from a health systems and policy perspective. Data were obtained for 63 medicines and vaccines, generating 1134 records from all 17 autonomous communities. Twenty-two medicines were commercially available in Spain, whereas 39 required exceptional access mechanisms. Routine stock availability across all centres was reported in only 31.1% of valid records, while 52.8% reported no routine stock and 16.1% restricted availability to reference centres. Joint management by prescribing physicians and hospital pharmacy services was required in 72.1% of access procedures. Marked territorial variability was also observed in dispensing circuits and financing mechanisms, with 47.9% of valid records requiring full out-of-pocket payment and 47.1% involving co-payment. Access to essential medicines for NTDs in Spain remains structurally fragmented and territorially unequal. Strengthening coordinated national pharmaceutical policies is necessary to reduce reliance on exceptional access mechanisms and ensure equitable, timely, and sustainable access to essential medicines in Spain and other decentralised European health systems.

PubMedMediterranean journal of rheumatology2026-09-18

Vaccines for Autoimmune Diseases: Stopping Triggers, Restoring BalanceA Systematic Review with Qualitative Synthesis.

de Carvalho Jozélio Freire JF, Caldas Cezar Augusto Muniz CAM, Shoenfeld Yehuda Y

To critically review the scientific background on vaccines designed to prevent autoimmune diseases, including two main strategies: (1) vaccines directed against pathogens involved in triggering disease, including Epstein-Barr virus (EBV), enterovirus and Streptococcus pyogenes; and (2) tolerogenic vaccine approaches targeting the immune response to restore tolerance to self-antigens. We performed a thorough systematic review of clinical trials, observational studies, meta-analysis and pre-clinical data. A broad search was implemented in biomedical databases and gray literature. This systematic review was conducted with qualitative synthesis, given the heterogeneity of study designs, diseases, and outcomes. Two reviewers independently selected studies for inclusion and extracted data, using standard risk of bias and quality of evidence assessment tools. There were 68 studies, 36 in humans and 32 preclinical studies included. In the anti-infective area, options include gp350 vaccine for EBV (phase 2), mRNA based early-stage vaccines, a population-based study of the impact of rotavirus vaccination on type 1 diabetes incidence, and inactivated PRV-101 Coxsackie B strain vaccine; for rheumatic fever, phase 1 trials are providing evidence with vaccines such as StreptAnova and J8/S2. With regard to the tolerogenic line, tolerogenic DC-based and of myelin peptides vaccines have shown immune regulation in illnesses such as MS and RA, but do not yet demonstrate solid clinical evidence. Trigger infections vaccines are now nearing clinical use whereas tolerogenic vaccines constitute an attractive approach for the future. The combination of these approaches has the potential to inform future preventive and therapeutic strategies, but current evidence remains heterogeneous and largely early-stage, particularly for tolerogenic platforms.

PubMedThe Pediatric infectious disease journal2026-09-18

Unilateral Earlobe Edema in Acute Primary Epstein-Barr Virus Infection: A Possible Variant of Hoagland Sign.

Bocquet Marie-Sophie MS, Crisinel Pierre Alex PA, Coste Alix T AT, Opota Onya O et al.

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