Evidence map›Paper›PMID 25707963›Full record

ReviewJournal of clinical pharmacology2015

Beyond peptides and mAbs--current status and future perspectives for biotherapeutics with novel constructs.

Dalal AlDeghaither, Brandon G Smaglo, Louis M Weiner

Open access · greenAbstract readReview
In one paragraph

Review in Journal of clinical pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.6field-weighted citation impact, top 5% 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.

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

26 citing papers in PubMed, 63 citations in OpenAlex.

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  16. Cysteine Residues inMicroorganisms · 2020
    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

3 authors at 2 institutions in 1 country.

Dalal AlDeghaitherGeorgetown Lombardi Comprehensive Cancer Center, Department of Oncology, Georgetown University Medical Center, Washington, DC, USA.
Brandon G Smaglo
Louis M Weiner
Georgetown University · USGeorgetown University Medical Center · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
TARGETED IMMUNOTHERAPY USING BISPECIFIC ANTIBODIESR01CA050633 · NCI · GEORGETOWN UNIVERSITY · PI WEINER, LOUIS M. · 1989 to 2018
$6.5M
ENGINEERED ANTIBREAST CANCER SINGLE-CHAIN FV IMMUNOTOXINU01CA051880 · NCI · NOVARTIS VACCINES AND DIAGNOSTICS, INC. · PI HOUSTON, L L · 1990 to 1994
–
NCI NIH HHS CA50633NCI NIH HHS CA51880NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA050633
6 · The paper itself

Abstract

Biotherapeutics are attractive anti-cancer agents due to their high specificity and limited toxicity compared to conventional small molecules. Antibodies are widely used in cancer therapy, either directly or conjugated to a cytotoxic payload. Peptide therapies, though not as prevalent, have been utilized in hormonal therapy and imaging. The limitations associated with unmodified forms of both types of biotherapeutics have led to the design and development of novel structures, which incorporate key features and structures that have improved the molecules' abilities to bind to tumor targets, avoid degradation, and exhibit favorable pharmacokinetics. In this review, we highlight the current status of monoclonal antibodies and peptides, and provide a perspective on the future of biotherapeutics using novel constructs.

Indexed as

AnimalsAntibodies, MonoclonalBiological ProductsHumansImmunoconjugatesNeoplasmsPeptidesAntibodies, MonoclonalBiological ProductsImmunoconjugatesPeptidesantibodiesantibody engineeringimmunoconjugatepeptides

Identifiers

PMID25707963
PMCPMC4340091
OpenAlexW1966732899

What OpenQuestion holds

Textmetadata
LicenceTDM
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.