Evidence map›Paper›PMID 37896976›Full record

ReviewVaccines2023

Novel Influenza Vaccines: From Research and Development (R&D) Challenges to Regulatory Responses.

Xiangchuan He, Tianxiang Zhang, Shitong Huan, Yue Yang

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. MedComm · 2024
    Article
  7. Bio-entrepreneurs' bugbear: Regulatory rigmarole.Perspectives in clinical research
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Xiangchuan HeSchool of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China.
Tianxiang ZhangSchool of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China.
Shitong HuanChina Office, The Bill & Melinda Gates Foundation, Beijing 100084, China.
Yue YangSchool of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China.
National Medical Products Administration · CNTsinghua University · CN

Funding

Bill and Melinda Gates Foundation grant INV-046112
6 · The paper itself

Abstract

Influenza vaccines faced significant challenges in achieving sufficient protective efficacy and production efficiency in the past. In recent decades, novel influenza vaccines, characterized by efficient and scalable production, advanced platforms, and new adjuvant technologies, have overcome some of these weaknesses and have been widely licensed. Furthermore, researchers are actively pursuing the development of next-generation and universal influenza vaccines to provide comprehensive protection against potential pandemic subtypes or strains. However, new challenges have emerged as these novel vaccines undergo evaluation and authorization. In this review, we primarily outline the critical challenges and advancements in research and development (R&D) and highlight the improvements in regulatory responses for influenza vaccines.

Indexed as

influenza pandemicsnovel influenza vaccinesprior licensingregulatory pathwaysresearch and development (R&D) challenges

Identifiers

PMID37896976
PMCPMC10610648
OpenAlexW4387453317

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.