Evidence map›Paper›PMID 38448430›Full record

ArticleNature communications2024

Development of ISB 1442, a CD38 and CD47 bispecific biparatopic antibody innate cell modulator for the treatment of multiple myeloma.

C Grandclément, C Estoppey, E Dheilly, M Panagopoulou, T Monney, C Dreyfus, J Loyau, V Labanca, A Drake, S De Angelis and 20 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 16 citations in OpenAlex.

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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 5 institutions in 4 countries.

C Grandclément *Ichnos Glenmark Innovation, Lausanne, CH, Switzerland.ORCID 0009-0005-3545-8243
C Estoppey *Ichnos Glenmark Innovation, Lausanne, CH, Switzerland.
E Dheilly *Ichnos Glenmark Innovation, Lausanne, CH, Switzerland.
M PanagopoulouIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
T MonneyIchnos Glenmark Innovation, Lausanne, CH, Switzerland.ORCID 0000-0002-8566-541X
C DreyfusIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
J LoyauIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
V LabancaIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
A DrakeIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
S De AngelisIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
A RubodIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
J FreiIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
L N CaroIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
S BleinIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
E MartiniIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
M ChimenIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
T MatthesHaematology Service, Department of Oncology and Clinical Pathology Service, Department of Diagnostics, University Hospital Geneva, 1211, Geneva, Switzerland.ORCID 0000-0002-4875-2477
Z KayaNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Institute, University of Oxford, Oxford, UK.
C M EdwardsNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Institute, University of Oxford, Oxford, UK.ORCID 0000-0002-1257-5659
J R EdwardsNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Institute, University of Oxford, Oxford, UK.ORCID 0000-0001-7391-0820
E MenoretNantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, Nantes, France.
C KervoelenNantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, Nantes, France.
C Pellat-DeceunynckNantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, Nantes, France.ORCID 0000-0002-6287-8148
P MoreauNantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, Nantes, France.
M L MbowIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
A SrivastavaIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
M R DysonIchnos Glenmark Innovation, Lausanne, CH, Switzerland.ORCID 0000-0002-8382-0789
E A ZhukovskyIchnos Glenmark Innovation, Lausanne, CH, Switzerland.
M Perro *Ichnos Glenmark Innovation, Lausanne, CH, Switzerland. mario.perro@iginnovate.com.ORCID 0000-0003-1375-8155
S Sammicheli *Ichnos Glenmark Innovation, Lausanne, CH, Switzerland. stefano.sammicheli@iginnovate.com.ORCID 0000-0002-7319-696X
Glenmark Pharmaceuticals (Switzerland) · CHCentre National de la Recherche Scientifique · FRNuffield Orthopaedic Centre · GBIchnos Sciences (United States) · USUniversity Hospital of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody engineering can tailor the design and activities of therapeutic antibodies for better efficiency or other advantageous clinical properties. Here we report the development of ISB 1442, a fully human bispecific antibody designed to re-establish synthetic immunity in CD38+ hematological malignancies. ISB 1442 consists of two anti-CD38 arms targeting two distinct epitopes that preferentially drive binding to tumor cells and enable avidity-induced blocking of proximal CD47 receptors on the same cell while preventing on-target off-tumor binding on healthy cells. The Fc portion of ISB 1442 is engineered to enhance complement dependent cytotoxicity, antibody dependent cell cytotoxicity and antibody dependent cell phagocytosis. ISB 1442 thus represents a CD47-BsAb combining biparatopic targeting of a tumor associated antigen with engineered enhancement of antibody effector function to overcome potential resistance mechanisms that hamper treatment of myeloma with monospecific anti-CD38 antibodies. ISB 1442 is currently in a Phase I clinical trial in relapsed refractory multiple myeloma.

Indexed as

Antibodies, BispecificHematologic NeoplasmsMultiple MyelomaAntibody-Dependent Cell CytotoxicityCD47 AntigenHumansAntibodies, BispecificCD47 AntigenCD47 protein, human

Identifiers

PMID38448430
PMCPMC10917784
OpenAlexW4392520395

What OpenQuestion holds

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LicenceCC BY
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.