Clinical Pharmacology Characterization of the First‐In‐Class Oncolytic Viral Therapy T‐VEC in Adults and Pediatric Subjects.

Oncolytic viruses are an emerging class of immunotherapies for cancer treatment. Talimogene laherparepvec (T‐VEC) is a first‐in‐class oncolytic virus approved globally for advanced melanoma. Herein, we describe the quantitative clinical pharmacology aspects of T‐VEC that supported the development of...

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Publicado en:Journal of Clinical Pharmacology Vol. 66; no. 1; pp. 1 - 14
Autores principales: Zhang, Xinwen, Balu, Bhavya, Chen, Po‐Wei, Mehta, Khamir, Li, Chuang, Upreti, Vijay V.
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell Jan2026
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2026
      vid: 66
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1002/jcph.70102
        191106116
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        atl: Clinical Pharmacology Characterization of the First‐In‐Class Oncolytic Viral Therapy T‐VEC in Adults and Pediatric Subjects.
      aug:
        au:
          Zhang, Xinwen
          Balu, Bhavya
          Chen, Po‐Wei
          Mehta, Khamir
          Li, Chuang
          Upreti, Vijay V.
        affil: Clinical Pharmacology, Modeling and Simulation, Amgen Inc., South San Francisco CA,, USA
      sug:
        subj:
          Oncolytic Virotherapy
          Immunotherapy
          Biological Products
          Neoplasms Drug Therapy
          Antineoplastic Agents Pharmacokinetics
          Antineoplastic Agents Pharmacodynamics
          Melanoma Drug Therapy
          Treatment Outcomes
          Human
          Funding Source
          Male
          Female
          Adolescence
          Adult
          Middle Age
          Aged
          Quantitative Studies
          Dose-Response Relationship, Drug
          Descriptive Statistics
          ROC Curve
          Mann-Whitney U Test
          Nonparametric Statistics
          Polymerase Chain Reaction
          Models, Theoretical
          Disease Progression
          Neoplastic Processes
          Drug Toxicity
          Drug Monitoring
          Childhood Neoplasms
          Patient Safety
          Pediatric Care
          Drug Development
          Risk Assessment
          Herpesviruses
          Adolescent: 13-18 years
          Adult: 19-44 years
          Middle Aged: 45-64 years
          Aged: 65+ years
          Male
          Female
      ab: Oncolytic viruses are an emerging class of immunotherapies for cancer treatment. Talimogene laherparepvec (T‐VEC) is a first‐in‐class oncolytic virus approved globally for advanced melanoma. Herein, we describe the quantitative clinical pharmacology aspects of T‐VEC that supported the development of this unique therapy. As a live therapy, the exposure characteristics of T‐VEC are vastly different from the pharmacokinetics (PK) of traditional small molecules or therapeutic proteins and were characterized as tumor site oncolytic viral kinetics. Relatively flat relationships between T‐VEC dose, lesion exposures, and efficacy were identified based on dose–exposure–response (D‐E‐R) analyses of 60 adult subjects, indicating that optimal drug effect was achieved over the studied dose range (106‐108 plaque forming unit [PFU]/mL); hence, efficacy was not sensitive to dose variations within the range. The relatively flat D‐E‐R relationship for T‐VEC was also beneficial for biopharmaceutic aspects unique for live viruses, including bridging small variations in viral infectivity observed from batch to batch during manufacturing. Additionally, the exposures in pediatric subjects (N = 15) were within the range, although generally lower in medians than adults (N = 60). The primary safety concern of T‐VEC‐related herpetic infection was evaluated using a mechanistic PK‐PD model which indicated minimal infection risk over the up to 5 years follow‐up duration. Overall, T‐VEC demonstrated favorable PK‐PD profiles and was well tolerated in adults and pediatric subjects at the approved dosing regimen. Quantitative clinical pharmacology analyses have supported the optimal development of T‐VEC and are poised to accelerate the development of these promising therapeutic oncolytic viruses.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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