Evidence map›Paper›PMID 41290704›Full record

ArticleNPJ vaccines2025

One year follow up of phase 1/2 randomized, placebo controlled trial of NDV-HXP-S vaccine in Thailand.

Weerapong Phumratanaprapin, Viravarn Luvira, Saranath Lawpoolsri, Juthaporn Cowan, Sant Muangnoicharoen, Supitcha Kamolratanakul, Yupa Sabmee, Piengthong Narakorn, Somchaiya Surichan, Laina D Mercer and 6 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Weerapong PhumratanaprapinVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Viravarn LuviraVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Saranath LawpoolsriDepartment of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Juthaporn CowanVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Sant MuangnoicharoenVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Supitcha KamolratanakulVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Yupa SabmeeVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Piengthong NarakornThe Government Pharmaceutical Organization, Bangkok, Thailand.
Somchaiya SurichanThe Government Pharmaceutical Organization, Bangkok, Thailand.
Laina D MercerPATH, Seattle, WA, USA.
Rama RaghunandanPATH, Seattle, WA, USA.
Christina S PolyakPATH, Seattle, WA, USA.
Ponthip WirachwongThe Government Pharmaceutical Organization, Bangkok, Thailand.
Jorge FloresPATH, Seattle, WA, USA.
Bruce L InnisPATH, Seattle, WA, USA.
Punnee PitisuttithumVaccine Trial Centre, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand. punnee.pit@mahidol.ac.th.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To promote self-reliance in vaccine production, a chimeric Newcastle Disease Virus (NDV) based vaccine (NDV-HXP-S) was developed in Bangkok, Thailand, with the support of PATH. The interim results of phase 1 on initial safety and immune responses of five formulations: 1 µg, 3 µg, 10 µg, 1 µg+ CpG, and 3 µg+CpG adjuvant were reported. The 3 µg and 3 µg+CpG formulations were selected to advance into phase 2. The full one-year follow-up of safety and immune responses of the NDV-HXP-S vaccine from a pooled phase 1/2 randomized, double-blind, placebo-controlled trial in vaccine naïve individuals with no prior SARS-CoV-2 infection was reported here. The two-dose NDV-HPX-S primary series was safe and elicited a strong immune response over one year, especially in the 3 µg+CpG and 10 µg groups. The 3 µg+CpG group had a significantly higher geometric mean fold rise (GMFR) than the 3 µg group (57.1 vs 40.0, p = 0.028) 14 days after the second dose.

Identifiers

PMID41290704
PMCPMC12722293

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.