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Record W4310161323 · doi:10.1182/blood-2022-168140

A First in Class, Open-Label, First-in-Human, Phase I Trial of Daily Oral Pclx-001

2022· article· en· W4310161323 on OpenAlexaff
Randeep Sangha, Laurie H. Sehn, Rahima Jamal, Jennifer L. Spratlin, John Kuruvilla, Michael J. Weickert, Luc G. Berthiaume, John R. Mackey

Bibliographic record

VenueBlood · 2022
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicUbiquitin and proteasome pathways
Canadian institutionsAlberta Cancer FoundationPrincess Margaret Cancer CentreUniversity Health NetworkCentre Hospitalier de l’Université de MontréalSpinal Cord Injury BCUniversity of British ColumbiaUniversity of Alberta
Fundersnot available
KeywordsTolerabilityMedicinePharmacokineticsPharmacologyInternal medicineToxicityOncologyLymphomaAdverse effectGastroenterology

Abstract

fetched live from OpenAlex

Background: Myristoylation regulates numerous membrane-bound signal transduction pathways important in cancer biology. This modification is catalyzed by N-myristoyltransferases 1 and 2 (NMT1 and NMT2). PCLX-001 is an oral small molecule with high affinity for both NMT proteins (IC50 of 5nM and 8nM, respectively) with high bioavailability. In vitro, cell lines of hematologic cancer origin were exquisitely sensitive to PCLX-001. PCLX-001 regressed subcutaneous tumors in murine xenograft models derived from lymphoma cell lines, as well as in a patient derived xenograft model from a patient with refractory DLBCL. The primary objective of this study is to determine the MTD and/or recommended phase II dose, safety, tolerability, and pharmacokinetics of PCLX-001 as a single agent in patients with refractory lymphomas and advanced solid tumors. Methods and Results: We are accruing to a multicenter, open-label, phase I dose-escalation study of daily oral PCLX-001 comprised of two parts (dose escalation and dose expansion). Eligible patients have histologically-confirmed advanced solid tumor or B-cell lymphomas who have failed prior therapy and/or are not eligible for therapies; ages ≥ 18 years; adequate organ function; life expectancy of at least 12 weeks; and measurable disease. Dose escalation has proceeded through 20 mg, 40 mg, 70 mg and 100 mg with each cohort achieving dose proportional pharmacokinetics without dose limiting toxicity. Three patients have been treated at each dose level of 20 mg, 40 mg, and 70 mg and five patients were treated in the 100 mg cohort. To date no dose limiting toxicities, neutropenia, or other safety signals have been observed. Noncompartmental pharmacokinetic analyses demonstrate an apparent terminal half-life of 8.5+/- 3h, rapid achievement of steady state and no PCLX-001 accumulation or induction of metabolism. PCLX-001 trough plasma concentrations at the higher dose cohorts exceed the EC90 required to inhibit cultured hematologic cells. Dose expansion in twenty patients with relapsed/refractory B-cell lymphoma will follow identification of the PCLX-001 maximally tolerated dose. Conclusions: Our results support the ongoing development of PCLX-001 as an oral, daily anticancer therapy. Updated study results will be presented, summarizing the safety and efficacy outcomes in PCLX-001 treated patients.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Non-randomized trial · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.020

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0000.000
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0020.004
Insufficient payload (model declined to judge)0.0060.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.037
GPT teacher head0.304
Teacher spread0.268 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNon-randomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2022
Admission routes1
Has abstractyes

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