Evidence map›Paper›PMID 41860591›Full record

ReviewClinical pharmacology and therapeutics2026

Advances in Human Mass Balance Studies: An IQ Consortium Perspective on Current Practices and Emerging Trends.

Jason Boer, Ellen Cannady, Filip Cuyckens, Ulrike Glaenzel, Camille Granvil, Felix Huth, Alexander D James, Wenying Li, Céline Veau, Graeme Young and 15 more

Abstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Jason Boer *Incyte Corporation, 1801 Augustine Cut-Off, Wilmington, Delaware, USA.ORCID 0009-0008-5628-0028
Ellen Cannady *Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA.
Filip Cuyckens *Johnson & Johnson, Turnhoutseweg, 30, Beerse, Belgium.ORCID 0000-0003-4956-1418
Ulrike Glaenzel *PK Sciences, Novartis Pharma AG, Fabrikstrasse 14, WSJ-153 1.02, Basel, 4056, Switzerland.
Camille Granvil *Work supported at Gilead Sciences, Foster City, California, USA.
Felix Huth *PK Sciences, Novartis Pharma AG, 4056, Basel, Switzerland.ORCID 0000-0002-7121-4394
Alexander D James *PK Sciences, Novartis Pharma AG, Fabrikstrasse 14, WSJ-153 1.02, Basel, 4056, Switzerland.
Wenying Li *Work Supported at Bristol-Myers Squibb, Princeton, New Jersey, USA.ORCID 0009-0005-6340-8286
Céline Veau *Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany.
Graeme Young *GlaxoSmithKline Research & Development Ltd., David Jack Centre, Ware, UK.ORCID 0000-0003-1813-6072
Qin Yue *Work supported at Gilead Sciences, Foster City, California, USA.
Gregory S Walker *Pfizer, Groton, Connecticut, USA.ORCID 0000-0003-0129-1682
Upendra A ArgikarGates Medical Research Institute, Cambridge, Massachusetts, USA.
Jonathan N BaumanPfizer, Groton, Connecticut, USA.
Cathy CantalloubeSanofi, Vitry sur Seine, France.ORCID 0000-0002-3083-5362
Yu-Luan ChenSumitomo Pharma America, Marlborough, Massachusetts, USA.ORCID 0000-0002-2866-3602
Ping KangVertex Pharmaceuticals, San Diego, California, USA.
Patricia MolinerSanofi, Montpellier, France.
Mette L PedersenDrug Metabolism and Pharmacokinetics, Early Research and Development, Cardiovascular, Renal and Metabolism, Biopharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Isabel PielBayer AG, Wuppertal, Germany.ORCID 0000-0002-6745-3069
Simone SchadtRoche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche, Basel, Switzerland.
Hanno SchiefersteinThe Healthcare Business of Merck KGaA, Darmstadt, Germany.
Julia Suchomel1 DNA Way, MS 412a, DMPK, Genentech, Inc., South San Francisco, California, USA.
Shuai Wang1 DNA Way, MS 412a, DMPK, Genentech, Inc., South San Francisco, California, USA.
S Cyrus Khojasteh *1 DNA Way, MS 412a, DMPK, Genentech, Inc., South San Francisco, California, USA.ORCID 0000-0002-8385-9288

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human radiolabeled mass balance studies are crucial for comprehensively characterizing the absorption, distribution, metabolism, and excretion (ADME) of investigational drugs, providing essential data for drug development, regulatory evaluation, and product labeling. The IQ Consortium's Human Mass Balance Radiolabeled ADME (hADME) Working Group developed this perspective to address key considerations and highlight opportunities for these studies. This is particularly relevant as regulatory guidance, such as the 2024 US Food and Drug Administration (FDA) and China's National Medical Products Administration (NMPA), have finalized dedicated guidance documents, along with recommendations from other global regulatory bodies (including European Medicines Agency (EMA) and Pharmaceuticals and Medical Devices Agency (of Japan; PMDA)); still, there are some regional differences. This review outlines current practices and emerging trends in hADME study design. It details seven clinical designs, from conventional radiolabeled approaches to microtracer studies that employ analytical techniques, such as accelerator mass spectrometry (AMS). It further highlights alternative non-radioactive approaches, including the use of Fluorine-19 nuclear magnetic resonance (

Indexed as

Drug DevelopmentDrugs, InvestigationalBiological AvailabilityHumansUnited StatesUnited States Food and Drug AdministrationDrugs, Investigational

Identifiers

PMID41860591
PMCPMC13264464

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.