Recent Updates
Recently added Catalysts
TRVI Positive Sentiment Score: 65/100

Trevi Therapeutics to Report Q1 2023 Financial Results and Provide a Corporate Update on May 11, 2023 Trevi Therapeutics, Inc. (Nasdaq: TRVI), a clinical-stage biopharmaceutical company developing the investigational therapy Haduvio™ (oral nalbuphine...

Key Takeaway: Trevi Therapeutics, Inc. will report its Q1 2023 financial results on May 11, 2023, during a conference call and webcast. The company is focused on its investigational therapy, Haduvio, aimed at treating chronic cough in patients with idiopathic pulmonary fibrosis (IPF) and prurigo nodularis. This event will provide a corporate update and an overview of the company's financial performance for the first quarter. Interested parties can access the conference call via phone or live audio webcast from Trevi's website.

Market Sentiment Analysis

POSITIVE FACTORS

  • Trevi Therapeutics is progressing with Haduvio's development for chronic cough and prurigo nodularis.
  • The upcoming conference call indicates active engagement with investors regarding corporate developments.
  • Haduvio could address significant medical needs in chronic cough treatment.

Full Press Release Details

Conference call and webcast to be held at 4:30 p.m. EDT
NEW HAVEN, Conn. , May 4, 2023 /PRNewswire/ -- Trevi Therapeutics, Inc. (Nasdaq: TRVI ), a clinical-stage biopharmaceutical company developing the investigational therapy Haduvio™ (oral nalbuphine ER) for the treatment of chronic cough in adults with idiopathic pulmonary fibrosis (IPF) and other chronic cough indications, and for the treatment of prurigo nodularis, today announced that senior management will host a conference call and live audio webcast on Thursday, May 11, 2023, at 4:30 p.m. ET, to provide a corporate update and review the Company's financial results for the first quarter ended March 31, 2023 .
To participate in the live conference call by phone, please dial (888) 317 6003 (domestic) or (412) 317 6061 (international) and provide access code 0161285. A live audio webcast will be accessible from the 'Investors & News' section on the Company's website at www.TreviTherapeutics.com . An archived replay of the webcast will also be available for 30 days on the Company's website following the event.
About Trevi Therapeutics, Inc. Trevi Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing Haduvio, an investigational therapy in an oral extended-release formulation of nalbuphine, for the treatment of chronic cough in IPF and other chronic cough indications. Haduvio is a mixed ĸ-opioid receptor agonist and µ-opioid receptor antagonist that works both centrally and peripherally. The ĸ and µ receptors are known critical mediators of cough. Parenteral nalbuphine has been approved and marketed for over 20 years for the treatment of acute pain indications and is not scheduled by the DEA in the United States or by regulatory authorities in most of Europe. Trevi intends to propose Haduvio as the trade name for nalbuphine ER. Its safety and efficacy have not been evaluated by any regulatory authority.
For more information, visit www.TreviTherapeutics.com and follow Trevi on Twitter and LinkedIn .
Investor Contact Katie McManus Trevi Therapeutics, Inc. 203-304-2499 [email protected]
Media Contact Rosalia Scampoli 914-815-1465 [email protected]
SOURCE Trevi Therapeutics, Inc.

21 %

Frequently Asked Questions

What is Haduvio developed by Trevi Therapeutics?

Haduvio is an investigational oral extended-release nalbuphine therapy for chronic cough and prurigo nodularis.

When will Trevi Therapeutics hold its conference call?

The conference call is scheduled for May 11, 2023, at 4:30 p.m. EDT.

How can I access the conference call?

Participants can dial (888) 317 6003 domestically or (412) 317 6061 internationally.

Is there a replay available after the conference call?

Yes, an archived replay will be available for 30 days on Trevi's website.

Has Haduvio been evaluated for safety and efficacy?

No, Haduvio's safety and efficacy have not been evaluated by any regulatory authority.

Last updated: May 4, 2023