Evidence map›Paper›PMID 33045114›Full record

ArticleJournal of clinical pharmacology2020

Assessment of Clinical Drug-Drug Interactions of Elagolix, a Gonadotropin-Releasing Hormone Receptor Antagonist.

Akshanth R Polepally, Juki W Ng, Ahmed Hamed Salem, Matthew B Dufek, Apurvasena Parikh, David C Carter, Kent Kamradt, Nael M Mostafa, Mohamad Shebley

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Combined Oral Contraceptives As Victims of Drug Interactions.Drug metabolism and disposition: the biological fate of chemicals · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
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

9 authors at 1 institution in 1 country.

Akshanth R PolepallyClinical Pharmacology and Pharmacometrics, AbbVie Inc., Redwood City, California, USA.ORCID 0000-0002-5938-6062
Juki W NgPharmaceutical Development, General Medicine, AbbVie Inc., North Chicago, Illinois, USA.
Ahmed Hamed SalemClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.ORCID 0000-0002-9261-1583
Matthew B DufekClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.
Apurvasena ParikhClinical Pharmacology and Pharmacometrics, AbbVie Inc., Redwood City, California, USA.
David C CarterClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.
Kent KamradtClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.
Nael M MostafaClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.
Mohamad ShebleyClinical Pharmacology and Pharmacometrics, AbbVie Inc., North Chicago, Illinois, USA.ORCID 0000-0002-0147-8933
AbbVie (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elagolix is an oral gonadotropin-releasing hormone receptor antagonist indicated for the management of endometriosis-associated pain and in combination with estradiol/norethindrone acetate indicated for the management of heavy menstrual bleeding associated with uterine leiomyomas (fibroids) in premenopausal women. Elagolix coadministered with estradiol/norethindrone acetate is in late-stage development for the management of heavy menstrual bleeding associated with uterine fibroids. Based on the in vitro profile of elagolix metabolism and disposition, 9 drug-drug interaction (DDI) studies evaluating the victim and perpetrator characteristics of elagolix were conducted in 144 healthy volunteers. As a victim of cytochrome P450 (CYPs) and transporter-mediated DDIs, elagolix area under the curve (AUC) increased by ∼2-fold following coadministration with ketoconazole and by ∼5- and ∼2-fold with single and multiple doses of rifampin, respectively. As a perpetrator, elagolix decreased midazolam AUC (90% confidence interval) by 54% (50%-59%) and increased digoxin AUC by 32% (23%-41%). Elagolix decreased rosuvastatin AUC by 40% (29%-50%). No clinically significant changes in exposure on coadministration with sertraline or fluconazole occurred. A elagolix 150-mg once-daily regimen should be limited to 6 months with strong CYP3A inhibitors and rifampin because of the potential increase in bone mineral density loss, as described in the drug label. A 200-mg twice-daily regimen is recommended for no more than 1 month with strong CYP3A inhibitors and not recommended with rifampin. Elagolix is contraindicated with strong organic anion transporter polypeptide B1 inhibitors (eg, cyclosporine and gemfibrozil). Consider increasing the doses of midazolam and rosuvastatin when coadministered with elagolix, and individualize therapy based on patient response. Clinical monitoring is recommended for P-glycoprotein substrates with a narrow therapeutic window (eg, digoxin). Dose adjustments are not required for sertraline, fluconazole, bupropion (or any CYP2B6 substrate), or elagolix when coadministered.

Indexed as

AdultATP Binding Cassette Transporter, Subfamily B, Member 1ATP Binding Cassette Transporter, Subfamily G, Member 2Cytochrome P-450 CYP2B6Cytochrome P-450 CYP2B6 InducersCytochrome P-450 CYP2C9 InhibitorsCytochrome P-450 CYP3ACytochrome P-450 CYP3A InducersCytochrome P-450 CYP3A InhibitorsDrug Administration ScheduleDrug InteractionsFemaleHealthy VolunteersHumansHydrocarbons, FluorinatedLiver-Specific Organic Anion Transporter 1ABCG2 protein, humanATP Binding Cassette Transporter, Subfamily B, Member 1ATP Binding Cassette Transporter, Subfamily G, Member 2CYP2B6 protein, humanCYP3A protein, humanCytochrome P-450 CYP2B6Cytochrome P-450 CYP2B6 InducersCytochrome P-450 CYP2C9 InhibitorsCytochrome P-450 CYP3ACytochrome P-450 CYP3A InducersCytochrome P-450 CYP3A InhibitorselagolixHydrocarbons, FluorinatedLiver-Specific Organic Anion Transporter 1Neoplasm ProteinsPyrimidinesReceptors, LHRHSLCO1B1 protein, humanSolute Carrier Organic Anion Transporter Family Member 1B3CYP3Adrug-drug interactionelagolixendometriosisGnRH antagonistuterine fibroids

Identifiers

PMID33045114
PMCPMC7689813
OpenAlexW3040663058

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.