ClinicalTrials.gg
CompletedNCT07324616Updated Jul 31, 2026

A Study to Evaluate EDG-7500 in Adults With Hepatic Impairment

A Phase 1 interventional study of EDG-7500 in Hepatic Impairment (HI), sponsored by Edgewise Therapeutics, Inc.. Completed at 2 sites in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-31.

Sponsored by Edgewise Therapeutics, Inc. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this Phase 1 study is to understand and compare the amount of EDG-7500 in the blood after a single dose in participants with different levels of liver function impairment versus participants with normal liver function. The safety of EDG-7500 in adult participants with different levels of liver function impairment will also be evaluated in this study.

02

Conditions studied

  • Hepatic Impairment (HI)

Keywords

  • Hepatic Impairment
03

In context

Lead sponsor

Edgewise Therapeutics, Inc. is the lead sponsor of 17 studies on the registry; 2 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 1 (8%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

All Participants

  • Adult, male or female, ≥ 18 years of age.
  • Female and male participants must follow protocol-specified guidance.
  • Continuous non-smoker or moderate smoker (≤ 10 cigarettes per day or equivalent) for at least 3 months prior to dosing.
  • ≥ 18.0 and ≤ 40.0 kg/m2 at screening.
  • >60 mL/min calculated using the 2021 CKD-EPI creatinine equation.

Participants with Mild and Moderate Hepatic Impairment (HI)

  • With the exception of HI, is in generally good health for study participation including the following:

    • Pulse rate is ≥ 40 bpm and ≤ 110 bpm at screening.
    • interval is ≤ 500 msec and has findings considered normal or not .
  • Has impaired hepatic function as defined by the classification for severity of liver disease and has a Child-Pugh score in line with one of the following HI cohorts at screening:

    • Mild HI (Class A): Child-Pugh score of 5 to 6, inclusive.
    • Moderate HI (Class B): Child-Pugh score of 7 to 9, inclusive.
  • Has a diagnosis of chronic (> 6 months), stable (no acute episodes of illness within the previous 2 months due to deterioration in hepatic function) hepatic insufficiency.

Participants with Normal Hepatic Function:

-Medically healthy, including the following:

  • Blood pressure is ≥ 90/40 mmHg and ≤ 150/95 mmHg.
  • Pulse rate is ≥ 40 bpm and ≤ 100 bpm.
  • QTcF interval is ≤ 470 msec and has ECG findings considered normal or not clinically significant.
  • Liver function test including ≤ , AST ≤ ULN, and total ≤1.5x ULN.

Exclusion criteria

Exclusion Criteria:

All Participants

  • History or presence of alcohol or drug abuse within the past 1 year prior to dosing.
  • Female participant with a positive pregnancy test at the screening visit or at check-in or who is lactating or breastfeeding.
  • Positive urine or breath alcohol results at screening or check-in. Unable to refrain from or anticipates the use of any drugs.
  • Positive results for at screening.
  • Donation of blood or significant blood loss within 56 days prior to dosing.
  • Plasma donation within 7 days prior to dosing.
  • Participation in another clinical study within 30 days or within 5 half-lives (if known), prior to dosing.

Participants with Mild and Moderate HI

  • With the exception of HI, history or presence of medical or psychiatric condition or disease, or any illness that might confound the results of the study or poses an additional risk to the participant by their participation in the study.
  • History of severe complications of liver disease within the preceding 3 months of screening.
  • Primary biliary cholangitis or biliary obstruction at screening.
  • Fluctuating or rapidly deteriorating hepatic function from screening until prior to dosing.
  • History of liver or other solid organ transplantation.
  • Requires paracentesis more often than 2 times per month.
  • Transjugular intrahepatic portosystemic shunt and/or has undergone portacaval shunting within 90 days prior to screening.
  • Received antiviral and/or immune modulating therapy for active hepatitis infection within 90 days prior to dosing.
  • Diabetic participants with > 8.5% at screening.
  • Positive for or HBcAb and has positive hepatitis B virus DNA at screening.
  • Positive for and has a detectable HCV viral load at screening.

Participants with Normal Hepatic Function

  • History or presence of clinically significant medical or psychiatric condition or disease, or any illness that might confound the results of the study or poses an additional risk to the participant by their participation in the study.
  • Alcohol consumption > 14 drinks per week for males (7 for females) within 45 days of screening.
  • Positive result for HBsAg or HCV at screening.
Terms in these criteria, in plain language(14)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Child-Pugh class

A score of how well the liver works in people with liver disease such as cirrhosis: class A is mild, B moderate and C severe.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
25 participants (actual)

Study arms

  • Experimental
    Healthy Adults

    Drug: EDG-7500

  • Experimental
    Mild Hepatic Impairment

    Drug: EDG-7500

  • Experimental
    Moderate Hepatic Impairment

    Drug: EDG-7500

Interventions

06

What researchers measure

Primary outcomes

  1. Area under the plasma concentration time-curve from time zero to the last measured concentration (AUC0-last)

    Time frame: Pre-dose to day 10

  2. Area under the plasma concentration time-curve from time zero extrapolated to infinity (AUC0-inf)

    Time frame: Pre-dose to day 10

  3. Maximum observed plasma concentration (Cmax)

    Time frame: Pre-dose to day 10

Secondary outcomes

  1. Safety: incidence of treatment-emergent adverse events

    To evaluate the safety and tolerability of a single oral dose of EDG-7500 in participants with mild and moderate hepatic impairment and participants with normal hepatic function

    Time frame: Up to 14 days of monitoring

07

Study locations

2 sites
  • The University of Miami Division of Clinical Pharmacology
    Miami, Florida 33136, United States
  • Orlando Clinical Research Center
    Orlando, Florida 32809, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2026 to primary completion in Apr 2026, 2 months.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 23, 2025
First posted
Jan 7, 2026
StartActual
Jan 26, 2026
Primary completionActual
Apr 7, 2026
CompletionActual
Apr 7, 2026
Last update
Jul 31, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07324616
Lead sponsor
Edgewise Therapeutics, Inc.
Responsible party
Sponsor
First posted
Jan 7, 2026
Start date
Jan 26, 2026
Primary completion
Apr 7, 2026
Completion
Apr 7, 2026
Last update
Jul 31, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: EDG-7500

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