Abstract 6703: Rg002: An mRNA-LNP-based immunotherapy targeting HPV-16/18-related malignancies

Abstract Prophylactic vaccines against oncogenic human papillomaviruses (HPVs) are effective in preventing HPV infection but not in treating existing HPV infection and cervical intraepithelial neoplasia (CIN). Current treatments for CIN are often ablative and may lead to long-term reproductive morbidity. Thus, there is a tremendous need for therapies that can treat the millions living with persistent oncogenic HPV infection and CIN and the risk of HPV-related cancers. RG002 is a mRNA-based therapeutic treatment targeting the E2, E6, and E7 proteins of HPV-16/18 with a targeted LNP for selective delivery to spleen and dendritic cells, which demonstrated excellent efficacy and safety in preclinical studies. In the phase I and expanded clinical studies, we evaluated the safety, efficacy, and immunogenicity of RG002 in 12 women with HPV 16/18 associated CIN2/3. Patients receive intramuscular administrations of 25, 75, 150, or 300 μg of RG002 at weeks 0, 2, and 4. RG002 does not cause any serious vaccine-related adverse events at any of the administered doses. Notably, all patients have exhibited complete regression of lesions and viral clearance within 17 weeks after the first dose, along with unprecedented E2/E6/E7 specific IFN-γ-producing T-cell response with clear dose-responses relationships. These initial data demonstrate the strong potential of RG002 as a first-in-class, non-surgical treatment for HPV-16/18-associated CIN2/3 to prevent progression to invasive carcinoma. Note on Study Status: *The initial cohort (n=12; 3 per dose) is nearing completion. Based on promising early results, the protocol has been amended to enroll an additional 15-30 patients by January 2026. Updated results from over 40 patients, including Week 17 efficacy data for at least 20 patients, are expected in mid-April 2026.* Citation Format: Shan Cen, Lan Zhu, Fei Chen, Wei Wang, Lihua Qiu, Hua Yang, Yijie Dong, Weiguo Zhang, Huizhen Zhang, Jing Wang. Rg002: An mRNA-LNP-based immunotherapy targeting HPV-16/18-related malignancies [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6703.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6703
Primary Topic
Cervical Cancer and HPV Research
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article
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article

Abstract 6703: Rg002: An mRNA-LNP-based immunotherapy targeting HPV-16/18-related malignancies

Yijie Dong, F. Chen, Huizhen Zhang, Wei Wang et al.
Cancer Research
Cervical Cancer and HPV Research
article

Abstract 6703: Rg002: An mRNA-LNP-based immunotherapy targeting HPV-16/18-related malignancies

Yijie Dong, F. Chen, Huizhen Zhang, Wei Wang, Lihua Qiu, Hua Yang, Jing Wang, Shan Cen, Weiguo Zhang
article en

Abstract

Abstract Prophylactic vaccines against oncogenic human papillomaviruses (HPVs) are effective in preventing HPV infection but not in treating existing HPV infection and cervical intraepithelial neoplasia (CIN). Current treatments for CIN are often ablative and may lead to long-term reproductive morbidity. Thus, there is a tremendous need for therapies that can treat the millions living with persistent oncogenic HPV infection and CIN and the risk of HPV-related cancers. RG002 is a mRNA-based therapeutic treatment targeting the E2, E6, and E7 proteins of HPV-16/18 with a targeted LNP for selective delivery to spleen and dendritic cells, which demonstrated excellent efficacy and safety in preclinical studies. In the phase I and expanded clinical studies, we evaluated the safety, efficacy, and immunogenicity of RG002 in 12 women with HPV 16/18 associated CIN2/3. Patients receive intramuscular administrations of 25, 75, 150, or 300 μg of RG002 at weeks 0, 2, and 4. RG002 does not cause any serious vaccine-related adverse events at any of the administered doses. Notably, all patients have exhibited complete regression of lesions and viral clearance within 17 weeks after the first dose, along with unprecedented E2/E6/E7 specific IFN-γ-producing T-cell response with clear dose-responses relationships. These initial data demonstrate the strong potential of RG002 as a first-in-class, non-surgical treatment for HPV-16/18-associated CIN2/3 to prevent progression to invasive carcinoma. Note on Study Status: *The initial cohort (n=12; 3 per dose) is nearing completion. Based on promising early results, the protocol has been amended to enroll an additional 15-30 patients by January 2026. Updated results from over 40 patients, including Week 17 efficacy data for at least 20 patients, are expected in mid-April 2026.* Citation Format: Shan Cen, Lan Zhu, Fei Chen, Wei Wang, Lihua Qiu, Hua Yang, Yijie Dong, Weiguo Zhang, Huizhen Zhang, Jing Wang. Rg002: An mRNA-LNP-based immunotherapy targeting HPV-16/18-related malignancies [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6703.

Cancer ResearchVol. 86(7_Supplement)
Universidade Estadual de Londrina (BR), Shanxi Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN), Tongren Hospital (CN), Second Hospital of Shanxi Medical University (CN)
Good health and well-being
Openalex Percentile: Top 19%
Cervical Cancer and HPV Research
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