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Merck Highlights Data On New Vaccine, Compares 'Tolerability And Safety' To Pfizer's

Merck Highlights Data On New Vaccine, Compares 'Tolerability And Safety' To Pfizer's

默沙東重點介紹新疫苗數據,將 “耐受性和安全性” 與輝瑞的疫苗進行了比較
Benzinga ·  2023/11/29 01:03

Merck & Co Inc (NYSE:MRK) released results from the STRIDE-3 Phase 3 trial evaluating V116, the company's investigational 21-valent pneumococcal conjugate vaccine.

默沙東公司(紐約證券交易所代碼:MRK)發佈了評估該公司在研的21價肺炎球菌偶聯疫苗V116的 STRIDE-3 3期試驗結果。

The trial evaluated the immunogenicity, tolerability, and safety of V116 compared to Pfizer Inc's (NYSE:PFE) Prevnar 20 (PCV20) in adults who had not previously received a pneumococcal vaccine.

該試驗評估了V116與輝瑞公司(紐約證券交易所代碼:PFE)Prevnar 20(PCV20)在以前未接種過肺炎球菌疫苗的成年人中的免疫原性、耐受性和安全性。

In adults 50 years of age and older (Cohort 1), V116 elicited non-inferior immune responses compared to PCV20 for all 10 serotypes common to both vaccines as measured by serotype-specific opsonophagocytic activity (OPA) geometric mean titers (GMTs) at Day 30.

在50歲及以上的成年人(隊列1)中,根據血清型特異性食管細胞活性 (OPA) 幾何平均滴度 (GMT) 在第30天測量,與兩種疫苗共有的全部10種血清型相比,V116引起的免疫反應並不遜色。PCV20

In adults 18 to 49 (Cohort 2), V116 elicited non-inferior immune responses (immunobridged) compared to adults 50 to 64, as assessed by serotype-specific OPA GMTs 30 days post-vaccination.

根據疫苗接種後30天血清型特異性OPA GMTs的評估,在18至49歲的成年人(隊列2)中,與50至64歲的成年人相比,V116引起的免疫反應不遜色(免疫橋接)。

Across both cohorts, V116 had a safety profile comparable to PCV20.

在這兩個隊列中,V116 的安全性與 PCV20 相當。

The V116 Phase 3 clinical development program comprises eight trials (n=8,830) investigating the safety, tolerability, and immunogenicity of V116 in various adult populations.

V116 3期臨床開發計劃包括八項試驗(n=8,830),調查V116在不同成年人群中的安全性、耐受性和免疫原性。

V116 utilizes the CRM197 vaccine carrier protein, produced using Ligand Pharmaceuticals Incorporated (NASDAQ:LGND) patent-protected Pelican Expression Technology platform. If approved, Ligand is entitled to a royalty on worldwide net sales.

V116 採用 CRM197 疫苗載體蛋白,該蛋白使用受專利保護的 Ligand Pharmicals Incorporated Incorporated(納斯達克股票代碼:LGND)生產的。如果獲得批准,Ligand有權獲得全球淨銷售額的特許權使用費。

In July, Merck announced topline results from two Phase 3 trials evaluating V116 in vaccine-naïve and previously vaccinated individuals.

7月,默沙東公佈了兩項針對未接種疫苗和以前接種過疫苗的人群評估V116的三期試驗的總體結果。

Price Action: MRK shares are down 0.84% at $100.58 on the last check Tuesday.

價格走勢:週二MRK股價下跌0.84%,至100.58美元。

譯文內容由第三人軟體翻譯。


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