Evidence map›Paper›PMID 34942275›Full record

ReviewAdvanced drug delivery reviews2022

Translating a radiolabeled imaging agent to the clinic.

Gary L Griffiths, Crystal Vasquez, Freddy Escorcia, Jeff Clanton, Liza Lindenberg, Esther Mena, Peter L Choyke

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. A Primer on Radiopharmaceutical Therapy.International journal of radiation oncology, biology, physics · 2023
    Review
  4. Review
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

7 authors.

Gary L GriffithsClinical Research Directorate, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Frederick, MD, United States.
Crystal VasquezMolecular Imaging Branch, National Cancer Institute, Bethesda, MD, United States.
Freddy EscorciaMolecular Imaging Branch, National Cancer Institute, Bethesda, MD, United States.
Jeff ClantonIndependent Consultant, Nashville, TN, United States.
Liza LindenbergMolecular Imaging Branch, National Cancer Institute, Bethesda, MD, United States.
Esther MenaMolecular Imaging Branch, National Cancer Institute, Bethesda, MD, United States.
Peter L ChoykeMolecular Imaging Branch, National Cancer Institute, Bethesda, MD, United States. Electronic address: pchoyke@nih.gov.

Funding

Growth Factor Imaging and PhotoimmunotherapyZIABC010656 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHOYKE, PETER L · 2009 to 2024
$31.6M
Engineering HCC-selective PET agentZIABC011800 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ESCORCIA, FREDDY · 2018 to 2025
$10.6M
Growth Factor ImagingZ01BC010656 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHOYKE, PETER L · 2005 to 2008
$1.6M
Intramural NIH HHS Z01 BC010656
6 · The paper itself

Abstract

Molecular Imaging is entering the most fruitful, exciting period in its history with many new agents under development, and several reaching the clinic in recent years. While it is unusual for just one laboratory to take an agent from initial discovery through to full clinical approval the steps along the way are important to understand for all interested participants even if one is not involved in the entire process. Here, we provide an overview of these processes beginning at discovery and preclinical validation of a new molecular imaging agent and using as an exemplar a low molecular weight disease-specific targeted positron emission tomography (PET) agent. Compared to standard drug development requirements, molecular imaging agents may benefit from a regulatory standpoint from their low mass administered doses, they nonetheless still need to go through a series of well-defined steps before they can be considered for Phase 1 human testing. After outlining the discovery and preclinical validation approaches, we will also discuss the nuances of Phase 1, Phase 2 and Phase 3 studies that may culminate in an FDA general use approval. Finally, some post-approval aspects of novel molecular imaging agents are considered.

Indexed as

Drug ApprovalClinical Trials as TopicDrug DevelopmentHumansMolecular ImagingMolecular WeightOctreotideOrganometallic CompoundsPositron-Emission TomographyUnited StatesUnited States Food and Drug Administrationlutetium Lu 177 dotatateOctreotideOrganometallic CompoundsMolecular imagingPET imaging agentsPhase 1 studiesPhase 2 studiesToxicity studies

Identifiers

PMID34942275
PMCPMC8889912

What OpenQuestion holds

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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.