Evidence map›Paper›PMID 42243603›Full record

ReviewPharmaceutical medicine2026

Optimising Formulations for Paediatric Patients with Inherited Metabolic Disorders: The Case Study of Levocarnitine.

Stephen Tomlin, Chris Mühlhausen, Andriy Krendyukov, Anibh Martin Das

Abstract readReview
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In one paragraph

Review in Pharmaceutical medicine, 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

4 authors.

Stephen TomlinDirector Children's Medicines Research and Innovation Centre, Great Ormond Street Hospital for Children, London, WC1N 1EP, UK.
Chris MühlhausenDepartment of Paediatrics and Adolescent Medicine, University Medical Center, Georg-August University, Göttingen, Germany.
Andriy KrendyukovMedical Office, Aspire Pharma Ltd., 4 Rotherbrook Court, Bedford Road, Petersfield, Hampshire, UK. ankov.de@outlook.com.ORCID http://orcid.org/0000-0001-8557-1520
Anibh Martin DasDepartment of Paediatrics, Clinic for Paediatric Kidney, Liver- and Metabolic Diseases and Neuropaediatrics, Hannover Medical School, Carl Neuberg Str. 1, 30625, Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited metabolic disorders (IMDs) are rare genetic conditions that disrupt normal biochemical pathways, leading to potentially life-threatening metabolic imbalances. Early diagnosis, often through newborn screening, and treatment can significantly improve outcomes, but pharmacological management presents unique challenges that are amplified by developmental immaturity, altered pharmacokinetics, and heightened sensitivity to drug excipients. The selection of excipients becomes especially important in IMDs such as primary carnitine deficiency (PCD), where lifelong supplementation is required. Substances such as parabens, benzoates, saccharin sodium, propylene glycol, and ethanol are generally safe in adults, but may potentially contribute to metabolic crises or cumulative toxicity in neonates due to immature organ systems and altered metabolism. Current regulatory frameworks are addressing these concerns through guidelines, labelling revisions, and tools such as the STEP and SEEN databases, which compile paediatric safety data for excipients. Despite regulatory progress, significant gaps in excipient transparency, standardisation, and labelling persist, complicating clinical decision making. Healthcare providers often lack access to precise excipient concentrations and may unintentionally exceed safe thresholds in polypharmacy scenarios. This opinion paper underscores the critical need for age-appropriate, excipient-conscious drug formulations for children with IMDs. It advocates for improved regulatory oversight, increased formulation transparency, and interdisciplinary collaboration to minimise risk and enhance the safety of paediatric treatments, particularly for neonates requiring chronic therapy.

Indexed as

CarnitineExcipientsMetabolism, Inborn ErrorsMuscular DiseasesCardiomyopathiesChildDrug CompoundingHumansHyperammonemiaInfant, NewbornCarnitineExcipients

Identifiers

What OpenQuestion holds

Textmetadata
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.