Evidence map›Paper›PMID 35051209›Full record

Trial reportPloS one2022

Results of a phase 1, randomized, placebo-controlled first-in-human trial of griffithsin formulated in a carrageenan vaginal gel.

Natalia Teleshova, Marla J Keller, José A Fernández Romero, Barbara A Friedland, George W Creasy, Marlena G Plagianos, Laurie Ray, Patrick Barnable, Larisa Kizima, Aixa Rodriguez and 20 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02875119 (A Phase 1 Trial to Evaluate the Safety, Pharmacokinetics), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 7% 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.

NCT02875119 phase1completednot on this map

A Phase 1 Trial to Evaluate the Safety, Pharmacokinetics (PK) and Pharmacodynamics (PD) of PC-6500 (Griffithsin [GRFT] in a Carrageenan Gel) in Healthy Women

TypeinterventionalSponsorPopulation CouncilRan2017 to 2018Enrolled15ConditionsHIV InfectionArmsGriffithsin Gel, Placebo Gel
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Plant-Based Systems for Producing Therapeutic Proteins: Current Status and Future Prospects.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
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  15. Estradiol inhibits HIV-1Scientific reports · 2022
    Article
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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

30 authors at 9 institutions in 1 country.

Natalia TeleshovaCenter for Biomedical Research, Population Council, New York, New York, United States of America.ORCID 0000-0003-3169-4650
Marla J KellerDepartment of Medicine, Albert Einstein College of Medicine, Bronx, New York, United States of America.ORCID 0000-0003-0417-4000
José A Fernández RomeroCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Barbara A FriedlandCenter for Biomedical Research, Population Council, New York, New York, United States of America.
George W CreasyCenter for Biomedical Research, Population Council, New York, New York, United States of America.ORCID 0000-0002-6645-4238
Marlena G PlagianosCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Laurie RayDepartment of Medicine, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Patrick BarnableCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Larisa KizimaCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Aixa RodriguezCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Nadjet CornejalScience Department, Borough of Manhattan Community College, New York, New York, United States of America.ORCID 0000-0003-4515-0152
Claudia MeloScience Department, Borough of Manhattan Community College, New York, New York, United States of America.
Gearoff Cruz RodriguezScience Department, Borough of Manhattan Community College, New York, New York, United States of America.ORCID 0000-0002-9094-8713
Sampurna MukhopadhyayCenter for Biomedical Research, Population Council, New York, New York, United States of America.ORCID 0000-0002-1944-765X
Giulia CalendaCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Shweta U SinkarCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Thierry BonnaireCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Asa WesenbergCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Shimin ZhangCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Kyle KleinbeckCenter for Biomedical Research, Population Council, New York, New York, United States of America.ORCID 0000-0002-5979-2116
Kenneth PalmerUniversity of Louisville, Louisville, Kentucky, United States of America.
Mohcine AlamiCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Barry R O'KeefeDivision of Cancer Treatment and Diagnosis, Molecular Targets Program, Center for Cancer Research and Natural Products Branch, Developmental Therapeutics Program, National Cancer Institute, Frederick, Maryland, United States of America.ORCID 0000-0003-0772-4856
Patrick GillevetGeorge Mason University, Manassas, Virginia, United States of America.
Hong HurRockefeller University, New York, New York, United States of America.ORCID 0000-0002-4088-9188
Yupu LiangRockefeller University, New York, New York, United States of America.ORCID 0000-0003-4074-463X
Gabriela SantoneHarvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-7279-4653
Raina N FichorovaHarvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0002-9980-5735
Tamara KalirIcahn School of Medicine at Mount Sinai, New York, New York, United States of America.ORCID 0000-0002-2370-0961
Thomas M ZydowskyCenter for Biomedical Research, Population Council, New York, New York, United States of America.
Population Council · USBorough of Manhattan Community College · USAlbert Einstein College of Medicine · USHarvard University · USRockefeller University · USGeorge Mason University · USIcahn School of Medicine at Mount Sinai · USNational Cancer Institute · USUniversity of Louisville · US

Funding

Isolation of bioactive proteins from natural product extractsZIABC011472 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI OKEEFE, BARRY · 2012 to 2025
$7.8M
6 · The paper itself

Abstract

HIV pre-exposure prophylaxis (PrEP) is dominated by clinical therapeutic antiretroviral (ARV) drugs. Griffithsin (GRFT) is a non-ARV lectin with potent anti-HIV activity. GRFT's preclinical safety, lack of systemic absorption after vaginal administration in animal studies, and lack of cross-resistance with existing ARV drugs prompted its development for topical HIV PrEP. We investigated safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of PC-6500 (0.1% GRFT in a carrageenan (CG) gel) in healthy women after vaginal administration. This randomized, placebo-controlled, parallel group, double-blind first-in-human phase 1 study enrolled healthy, HIV-negative, non-pregnant women aged 24-45 years. In the open label period, all participants (n = 7) received single dose of PC-6500. In the randomized period, participants (n = 13) were instructed to self-administer 14 doses of PC-6500 or its matching CG placebo (PC-535) once daily for 14 days. The primary outcomes were safety and PK after single dose, and then after 14 days of dosing. Exploratory outcomes were GRFT concentrations in cervicovaginal fluids, PD, inflammatory mediators and gene expression in ectocervical biopsies. This trial is registered with ClinicalTrials.gov, number NCT02875119. No significant adverse events were recorded in clinical or laboratory results or histopathological evaluations in cervicovaginal mucosa, and no anti-drug (GRFT) antibodies were detected in serum. No cervicovaginal proinflammatory responses and no changes in the ectocervical transcriptome were evident. Decreased levels of proinflammatory chemokines (CXCL8, CCL5 and CCL20) were observed. GRFT was not detected in plasma. GRFT and GRFT/CG in cervicovaginal lavage samples inhibited HIV and HPV, respectively, in vitro in a dose-dependent fashion. These data suggest GRFT formulated in a CG gel is a safe and promising on-demand multipurpose prevention technology product that warrants further investigation.

Indexed as

Pre-Exposure ProphylaxisAdministration, IntravaginalAdolescentAdultCarrageenanDouble-Blind MethodFemaleHIV-1HIV InfectionsHumansMiddle AgedPapillomaviridaePapillomavirus InfectionsPlant LectinsVaginal Creams, Foams, and JelliesCarrageenangriffithsin protein, GriffithsiaPlant LectinsVaginal Creams, Foams, and Jellies

Identifiers

PMID35051209
PMCPMC8775213
OpenAlexW4205746422

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.