Evidence map›Paper›PMID 39119977›Full record

Trial reportClinical and translational science2024

Using exploratory pharmacokinetic and pharmacodynamic analyses to predict the probability of flu-like symptoms in healthy volunteers and patients with chronic hepatitis B treated with the toll-like receptor 7 agonist ruzotolimod.

Qiudi Jiang, Yuchen Zhang, Dan Duan, Sylvie Retout, Ruchi Upmanyu, Katerina Glavini, Miriam Triyatni, Yonghong Zhu, Joseph F Grippo, Yuyan Jin

Abstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
  2. Soft drugs: design principles and topical applications.Nature reviews. Drug discovery · 2026
    Review
  3. 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

10 authors.

Qiudi JiangRoche Innovation Center, Shanghai, China.ORCID 0009-0004-2351-145X
Yuchen ZhangRoche Innovation Center, Shanghai, China.
Dan DuanRoche Innovation Center, Shanghai, China.
Sylvie RetoutRoche Innovation Center, Basel, Switzerland.ORCID 0000-0003-4867-8438
Ruchi UpmanyuRoche Innovation Center, Welwyn, UK.
Katerina GlaviniRoche Innovation Center, Basel, Switzerland.ORCID 0000-0001-6789-8781
Miriam TriyatniRoche Innovation Center, Basel, Switzerland.ORCID 0009-0000-7991-6916
Yonghong ZhuRoche Innovation Center, Shanghai, China.ORCID 0009-0000-0858-1506
Joseph F GrippoRoche Innovation Center, New York, New York, USA.
Yuyan JinRoche Innovation Center, Shanghai, China.ORCID 0009-0005-4532-1988

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ruzotolimod (Toll-like receptor 7 (TLR7) agonist, RG7854) is an oral, small molecule immuno-modulator activating the TLR 7 and is being evaluated in patients with CHB. As with other TLR7 agonists, the study drug-related adverse events of flu-like symptoms have been reported in some participants during phase I studies with ruzotolimod. An exploratory analysis of the relationship between pharmacokinetic (PK)/pharmacodynamic (PD) and flu-like symptoms was performed in participants from two phase I studies including both healthy volunteers and NUC-suppressed CHB patients who received either single or multiple ascending doses of orally administered ruzotolimod. Linear and logistic regression were used to explore potential relationships between dose, flu-like symptoms, PK, and PD. Generalized linear regression was performed to predict the probability of flu-like symptoms of all intensities at different RO7011785 (the active metabolite of the double prodrug ruzotolimod) PK exposure. This analysis showed that single or multiple doses of ruzotolimod at ⩾100 mg, the immune PD (IFN-α, neopterin, IP-10, and the transcriptional expression of ISG15, OAS-1, MX1, and TLR7) responses increase with the RO7011785 PK exposure, which increases linearly with the doses from 3 mg to 170 mg of ruzotolimod. The analysis also showed that the probability of flu-like symptoms occurrence increases with PD responses (IFN-α and IP-10). Dose reduction of ruzotolimod can be an effective way to reduce the magnitude of PD response, thus reducing the probability of study drug-related flu-like symptoms occurrence at all intensity in the participants who are highly sensitive to PD activation and intolerant to flu-like symptoms.

Indexed as

Healthy VolunteersHepatitis B, ChronicToll-Like Receptor 7Administration, OralAdolescentAdultAntiviral AgentsDose-Response Relationship, DrugFemaleHumansInfluenza, HumanMaleMiddle AgedOrganic ChemicalsYoung AdultAntiviral AgentsOrganic ChemicalsRO7020531TLR7 protein, humanToll-Like Receptor 7

Identifiers

PMID39119977
PMCPMC11310849

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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.