28 Participants NeededMy employer runs this trial

Atirmociclib for Liver Disease

Recruiting at 2 trial locations
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores how the new drug, atirmociclib, behaves in the body and assesses its safety for people with various liver conditions. Participants will take the medicine orally, and researchers will collect blood samples to determine how the liver processes the drug. The trial suits adults with normal liver function or stable liver disease that doesn’t change quickly. Participants will spend about a week in the clinic, depending on their liver health, with follow-ups after discharge. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new drug.

Is there any evidence suggesting that atirmociclib is likely to be safe for humans?

Research has shown that atirmociclib has been studied for its safety and mechanism of action. Early results suggest it is generally well-tolerated. One study found that when combined with letrozole, a cancer treatment, atirmociclib maintained a good safety record over about two years of follow-up. Although considered safe, atirmociclib, like many medicines, can have side effects. Some other medicines in the same group (CDK4/6 inhibitors) have been linked to liver problems. However, this does not mean atirmociclib will cause the same issues. It is important to remember that researchers are still studying atirmociclib to fully understand its safety.12345

Why do researchers think this study treatment might be promising?

Atirmociclib is unique because it targets liver disease through a novel mechanism, acting as a cyclin-dependent kinase (CDK) inhibitor. While traditional treatments for liver disease often focus on managing symptoms or slowing disease progression through medications like antiviral drugs or steroids, Atirmociclib directly interferes with the cellular processes that contribute to liver damage. Researchers are excited about this treatment because it offers a new approach that could potentially halt or reverse liver disease at the cellular level, providing hope for more effective management of the condition.

What evidence suggests that atirmociclib might be an effective treatment for liver disease?

Research has shown that atirmociclib yields promising results for treating certain breast cancers. One study demonstrated that combining atirmociclib with another drug helped patients live longer without cancer progression. Another study found the treatment effective in shrinking or controlling tumors. Although these studies focused on breast cancer, they suggest that atirmociclib could be explored for other conditions, such as liver disease. By targeting specific proteins involved in cell growth, it might help manage liver issues. In this trial, participants will be divided into groups based on liver function—normal hepatic function, mild hepatic impairment, moderate hepatic impairment, and severe hepatic impairment—to understand how atirmociclib works in the body across different levels of liver health.36789

Who Is on the Research Team?

PC

Pfizer CT.gov Call Center

Principal Investigator

Pfizer

Are You a Good Fit for This Trial?

This trial is for adults aged 18 or older who weigh over 50 kg and have a BMI between 17.5 and 40. Participants can have normal liver function or stable mild, moderate, or severe liver disease.

Inclusion Criteria

BMI of 17.5-40 kg/m2 and total body weight >50 kg (110 lb)
I am able to understand and sign a consent form.
Willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures
See 2 more

Exclusion Criteria

I have a condition or past surgery that may affect how my body absorbs medicine.
I am not taking any medications that are not allowed in this study.
I do not have any serious blood, kidney, hormone, lung, stomach, heart, mental, nerve, or drug allergy issues.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a single oral dose of Atirmociclib and are monitored for pharmacokinetics

1-2 weeks
7-9 days in-clinic stay

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks
Contacted by phone or clinic visit

What Are the Treatments Tested in This Trial?

Interventions

  • Atirmociclib

Trial Overview

The study tests how the medicine atirmociclib is processed in people with different levels of liver health. All participants take the medicine by mouth, and blood samples are collected to measure drug levels over time.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Group I: Group 4: Severe Hepatic ImpairmentExperimental Treatment1 Intervention
Group II: Group 3: Moderate Hepatic ImpairmentExperimental Treatment1 Intervention
Group III: Group 2: Mild Hepatic ImpairmentExperimental Treatment1 Intervention
Group IV: Group 1: Normal Hepatic FunctionExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Pfizer

Lead Sponsor

Trials
4,712
Recruited
50,980,000+
Known For
Vaccine Innovations
Top Products
Viagra, Zoloft, Lipitor, Prevnar 13

Albert Bourla

Pfizer

Chief Executive Officer since 2019

PhD in Biotechnology of Reproduction, Aristotle University of Thessaloniki

Patrizia Cavazzoni profile image

Patrizia Cavazzoni

Pfizer

Chief Medical Officer

MD from McGill University

Citations

108 Long-Term Safety and Efficacy of First-Line Next ...

At 24.8 months of follow-up, atirmociclib plus letrozole continues to show favorable safety/tolerability and promising efficacy when used as first-line ...

Ribociclib - LiverTox - NCBI - NIH

In one study, 1% of recipients developed clinically apparent liver injury with jaundice, but all recovered. The liver injury arose after 3 to 5 ...

FOURLIGHT-1 Study Data Support Atirmociclib for HR+ ...

The FOURLIGHT-1 study found that atirmociclib plus Faslodex significantly improved progression-free survival in patients with HR+/HER2- ...

Atirmociclib - Drug Targets, Indications, Patents

This study seeks to provide a detailed characterization of the in vitro and in vivo metabolism of atirmociclib, utilizing human liver microsomes

Atirmociclib Plus Letrozole Demonstrates Preliminary ...

showed a 58.8% overall response rate and 94.1% clinical benefit rate in HR-positive, HER2-negative

Clinical Trial for Hepatic Impairment, Healthy ...

The purpose of this study to understand how the study medicine atirmociclib behaves in the body and how safe it is for people with different levels of liver ...

Management of hepatotoxicity associated with CDK4/6 ... - PMC

The observed trend of increased hepatotoxicity in patients treated with ribociclib (66.6%) compared to those receiving palbociclib (33.3%)

Palbociclib-Induced Hepatotoxicity in a Patient with ...

Although palbociclib is generally well-tolerated, rare cases of hepatotoxicity. Although elevated liver function tests (LFTs) were reported in clinical trials ...

Atirmociclib | PF-07220060

Atirmociclib | PF-07220060 is an investigational compound. Its safety and efficacy have not been established.