Evidence map›Paper›PMID 42411454›Full record

ReviewClinical pharmacology and therapeutics2026

From Executor to Orchestrator: The Pharmacology Scientist in the Age of Agentic AI.

Michael McCoy, Matthew McCoy

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

2 authors.

Michael McCoyDrug Metabolism and Pharmacokinetics & Modeling, Takeda Development Center Americas, Cambridge, Massachusetts, USA.
Matthew McCoyIndependent Researcher, Kansas City, Missouri, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug development productivity has not improved despite five decades of computational advancement, with the probability that a compound entering Phase I achieving regulatory approval remaining near 10%. Each automation wave increased throughput while leaving the interpretive bottleneck intact; scientists continued to formulate questions, evaluate outputs, and make advancement decisions regardless of how fast data accumulated upstream. Agentic AI systems capable of reasoning, planning, and executing multi-step analyses without continuous human instruction represent the first class of ubiquitous computational tools with the architectural potential to compress this bottleneck, but the implications extend beyond efficiency. As computational systems begin to perform interpretation, execution, and evaluation steps that previously required human judgment, the scientist's contribution shifts from conducting analyses to specifying objectives precise enough for autonomous execution and evaluating recommendations that may be difficult to verify independently. Whether this shift improves aggregate productivity depends on whether autonomous systems address the fundamental causes of clinical failure, including insufficient efficacy, inadequate safety prediction, and poor preclinical translation, rather than merely accelerating the analytical work surrounding them. This review examines what clinical pharmacology scientists must become as these systems enter routine practice. The competencies required for effective orchestration differ from those emphasized in traditional pharmaceutical training, and existing governance structures do not address the failure modes that accompany delegation of scientific judgment to autonomous systems. Whether this shift improves productivity or introduces new failure modes depends on governance and training investments that the field has not yet made.

Indexed as

Artificial IntelligenceDrug DevelopmentPharmacology, ClinicalHumans

Identifiers

PMID42411454
PMCPMC13339049

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.