#ATS2018 — Pamrevlumab Slows Fibrosis Progression, Improves Lung Function in IPF, Phase 2 Trial Shows

Written by Patricia Inácio, PhD |

PRAISE Phase 2 trial

Investigational Pamrevlumab halts the progression of lung fibrosis and improves lung function in patients with idiopathic pulmonary fibrosis (IPF), new results from the Phase 2 PRAISE trial show.

These results were recently presented in a series of poster presentations at the American Thoracic Society (ATS) 2018 in San Diego.

“We are excited to present additional analyses of the PRAISE Phase 2b trial that confirm and expand our understanding of positive safety and efficacy results with pamrevlumab, with statistically significant treatment effects in slowing IPF progression with encouraging results in both lung function (FVC) and in lung fibrosis (QLF) for the first time in a controlled study. This study demonstrates the therapeutic potential of pamrevlumab and, brings us one step closer to helping IPF patients,” Elias Kouchakji, MD, senior vice president of clinical development and drug safety at FibroGen, said in a press release.

Pamrevlumab, developed by San Francisco-based FibroGen, targets a specific factor — called connective tissue growth factor (CTGF) — known for its role in promoting fibrosis progression-related diseases, including IPF.

The PRAISE Phase 2b trial (NCT01890265) randomized 103 patients with mild to moderate IPF to receive either 30 mg/kg of pamrevlumab, delivered directly into the vein, or a placebo every three weeks. Treatment occurred over 45 weeks for a total of 16 infusions.

The study’s main objective was lung function, measured as changes in forced vital capacity (FVC) at weeks 12, 24, 36, and 48 compared with the beginning of the study. Additional objectives evaluated the progression of lung fibrosis, measured by quantitative high-resolution computed tomography (qHRCT), a noninvasive imaging technique, at weeks 24 and 48.

Researchers also assessed changes in health-related quality of life and safety.

Results showed that treatment with pamrevlumab halted lung fibrosis progression relative to the placebo group — quantitative lung fibrosis volume was 24.8 ml for pamrevlumab-treated patients versus 86.4 ml for the placebo group at week 24.

After 48 weeks, fibrosis in pamrevlumab-treated patients reached a volume of 75.4 ml, while placebo-treated patients had more than double the fibrosis burden, a volume of 151.5 ml.

A decrease in fibrosis progression with pamrevlumab correlated with better lung function, as shown by a reduction in the rate of decline in FVC.

“Data from HRCT analysis show a strong correlation between changes in fibrosis with the changes in FVC in patients treated with pamrevlumab, suggesting the promise of this antibody as an effective and well-tolerated therapy for IPF patients,” said Jonathan G. Goldin, MD, PhD, the trial’s lead investigator and a professor of radiology at UCLA Medical Center.

“These exciting results in a placebo-controlled Phase 2 study clearly demonstrate that quantitative imaging can be incorporated into IPF clinical trials and show that pamrevlumab appears to have a positive and measurable effect on disease pathology,” he said.

For a complete list of the four posters presented by FibroGen at ATS 2018, visit this link.

sharon housden avatar

sharon housden

how exiting is this, my husband has lung fibrosis will this new medication be available in the uk,if so when is this likely to happen. thank you

Reply
Ed avatar

Ed

PBI-4050!!!

Reply
Richard Grix avatar

Richard Grix

Are there going to be any more trial studies? If so, how can I get on a list of canidates?

Reply
Cooper Abrams avatar

Cooper Abrams

Great news. When will it be avaviable?

Reply
Peggy Pittman avatar

Peggy Pittman

When will this medication be made available? Is it considered to be better than Esbreit and Ofev?

Reply
David Collard avatar

David Collard

Sound like very good news, but when will it be on the market and when will local doctors become aware of Pamrevlumab? What time frame are expected?

Reply
Larry Blackstad avatar

Larry Blackstad

What is the application for trail participation process

Reply
Ellen Hays avatar

Ellen Hays

I’ll be discussing this hopeful wonder drug with my pulmonologist on my next visit!

Reply
jack m Petrill avatar

jack m Petrill

i have pulmonary fibrosis if there is a trial i could apply to

Reply
Suzanne Brennan avatar

Suzanne Brennan

I'm currently on Esbriet after being on OFEV for a year and a half. In your trials, do you have patients come off these two drugs or do you have some stay on one of them in additional to your new drug?

How soon will you be sourcing patients for the new trials?

Reply
Barbara Blair avatar

Barbara Blair

Will it also help someone who has IPf AND ALSO chf (cardiomopathy). I am on Ofev now hand had been for 3 years (oxygen at 6). Would anything change?

Reply
Décio Tavares Soares avatar

Décio Tavares Soares

Is it possible receive information about the next trial? I have IPF and i use Esbriet since 2 months ago.
Thanks

Reply

Leave a comment

Fill in the required fields to post. Your email address will not be published.

Comments are moderated. Once approved, your comment and username will be publicly visible. Please avoid sharing personal health information or other sensitive details.