Evidence map›Paper›PMID 41015990›Full record

ArticleClinical drug investigation2025

Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Efbemalenograstim Alfa (F-627), a Novel Long-Acting rhG-CSF, in Healthy Chinese Participants: An Open-Label, Single-Center Phase I Study.

Zhihai Cao, Yao Li, Denny Hou, Shufang Wang, Wei Yao, Gaochong Zhang, Jianmin Chen, Zhengwei Tang, Linda Song, Xingna Zhao and 4 more

Abstract readClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in Clinical drug investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

14 authors.

Zhihai Cao *School of Pharmacy, Anhui Medical University, Hefei, 230032, China.
Yao Li *School of Pharmacy, Anhui Medical University, Hefei, 230032, China.
Denny HouEvive Biotech Co., Ltd, Shanghai, 201315, China.
Shufang WangEvive Biotech Co., Ltd, Shanghai, 201315, China.
Wei YaoEvive Biotech Co., Ltd, Shanghai, 201315, China.
Gaochong ZhangEvive Biotech Co., Ltd, Shanghai, 201315, China.
Jianmin ChenEvive Biotech Co., Ltd, Shanghai, 201315, China.
Zhengwei TangEvive Biotech Co., Ltd, Shanghai, 201315, China.
Linda SongEvive Biotech Co., Ltd, Shanghai, 201315, China.
Xingna ZhaoEvive Biotech Co., Ltd, Shanghai, 201315, China.
Xiaoxiang ChuEvive Biotech Co., Ltd, Shanghai, 201315, China.
Xiaoyan WangEvive Biotech Co., Ltd, Shanghai, 201315, China.
Renshu LiEvive Biotech Co., Ltd, Shanghai, 201315, China.
Wei HuSchool of Pharmacy, Anhui Medical University, Hefei, 230032, China. huwei@ahmu.edu.cn.ORCID http://orcid.org/0000-0002-4809-7601

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesIn clinical practice, granulocyte colony-stimulating factor (G-CSF) is often used to lower infection risk and avoid poor outcomes from chemotherapy dose reduction or delay. Efbemalenograstim alfa (also known as F-627) is a non-pegylated but long-acting (once-per-cycle) recombinant human granulocyte colony-stimulating factor (rhG-CSF) compared with pegfilgrastim. This study was designed to obtain pharmacokinetic (PK)/pharmacodynamic (PD), safety, and tolerability data for F-627 in healthy Chinese participants.

methodsThis was a single-center, open-label phase I clinical study involving 24 healthy Chinese volunteers (sex ratio = 1:1). All the participants were administered a single subcutaneous injection of 20 mg F-627 into the abdomen.

resultsIn this study, 15 (62.5%) participants reported 28 treatment-related adverse events. PK/PD data showed that after a single 20 mg subcutaneous (SC) F-627 abdominal injection in healthy Chinese participants, serum concentrations peaked at 36 h post dose, while the absolute neutrophil count (ANC) peaked at 96 h. After peaking, F-627 serum levels decreased rapidly to low concentrations by 120 h, while ANC declined gradually to near baseline by day 15. Similar trends in serum concentration and ANC kinetics were seen between sex.

conclusionsThis phase I study showed that 20 mg F-627 was well tolerated and exhibited a favorable safety profile in a healthy Chinese population. The PK and PD data correlated well and were consistent across sex.

trial registrationThis trial was registered at the Chinese Clinical Trial Registry (chictr.org.cn) on 10 September 2024 (registration ID: ChiCTR2400089548).

Indexed as

FilgrastimGranulocyte Colony-Stimulating FactorAdultChinaFemaleHealthy VolunteersHumansInjections, SubcutaneousMaleMiddle AgedRecombinant ProteinsYoung AdultFilgrastimGranulocyte Colony-Stimulating FactorRecombinant Proteins

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Registered trials

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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.