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PIRS News and Press, Pieris Pharmaceuticals Inc. From 09/20/20

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Company Name: Pieris Pharmaceuticals Inc.
Stock Symbol: PIRS
Market: NASDAQ
Website: pieris.com

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PIRS - Pieris Pharmaceuticals Presents Updated Data from Phase 1 Monotherapy and Atezolizumab Combination Studies of 4-1BB/HER2 Bispecific PRS-343 at the European Society for Medical Oncology (ESMO) Virtual Congress 2020

Clinical benefit in both trials, including one confirmed complete response and three partial responses in the monotherapy trial and four confirmed partial responses in the atezolizumab combination trial Robust durability of response in both trials, including more than 18 months in the...

PIRS - 4 Penny Stocks To Watch In August 2020 Making New Highs

Will These High Volume Penny Stocks Make Higher Highs This Month? One of the quickest ways to find penny stocks is by looking at technical trends. As I’ve said in the past, sometimes volume and price will dictate momentum before fundamentals. While that type of action could stem from...

PIRS - Pieris Pharmaceuticals, Inc. (PIRS) CEO Steve Yoder on Q2 2020 Results - Earnings Call Transcript

Pieris Pharmaceuticals, Inc. (PIRS) Q2 2020 Earnings Conference Call August 10, 2020 08:00 AM ET Company Participants Tom Bures - Vice President of Finance Steve Yoder - President and Chief Executive Officer Ingmar Bruns - Senior Vice President and Head of Clinical Development ...

PIRS - Pieris Pharmaceuticals Reports Second Quarter 2020 Financial Results and Provides Corporate Update

Company to Host an Investor Conference Call on Monday, August 10, 2020 at 8:00 AM EDT PRS-060/AZD1402 phase 2a trial in asthma to start in fourth quarter Signed clinical trial collaboration agreement with Lilly for supply of ramucirumab for phase 2 trial of PRS-343 PRS-343 ph...

PIRS - Pieris Pharma teams up with Lilly in gastric cancer study

Pieris Pharmaceuticals (NASDAQ: PIRS )  has entered into a clinical trial collaboration and supply agreement with Eli Lilly (NYSE: LLY ) to evaluate the safety and efficacy of combining Pieris' PRS-343, a 4-1BB/HER2 bispecific for HER2-positive tumors, with Lilly's ramucirumab, a V...

PIRS - Pieris and Lilly Enter Into a Clinical Trial Collaboration to Evaluate Combination of PRS-343 With Ramucirumab and Paclitaxel in Gastric Cancer

BOSTON, MA / ACCESSWIRE / August 10, 2020 / Pieris Pharmaceuticals, Inc. (NASDAQ:PIRS) , a clinical-stage biotechnology company advancing novel biotherapeutics through its proprietary Anticalin ® technology platform for respiratory diseases, cancer, and other indications, toda...

PIRS - Pieris Pharmaceuticals to Host Second Quarter 2020 Investor Call and Corporate Update on August 10, 2020

BOSTON, MA / ACCESSWIRE / August 3, 2020 / Pieris Pharmaceuticals, Inc. (NASDAQ:PIRS) , a clinical-stage biotechnology company advancing novel biotherapeutics through its proprietary Anticalin® technology platform for respiratory diseases, cancer and other indications, today announced ...

PIRS - Pieris Pharmaceuticals Announces Oral Presentation of Phase 1 Data for 4-1BB/HER2 Bispecific PRS-343 at European Society for Medical Oncology (ESMO) Virtual Congress 2020

BOSTON, MA / ACCESSWIRE / July 23, 2020 / Pieris Pharmaceuticals, Inc. (NASDAQ:PIRS) , a clinical-stage biotechnology company advancing novel biotherapeutics through its proprietary Anticalin ® technology platform for respiratory diseases, cancer, and other indications, today announce...

PIRS - FDA suspends enrollment in Pieris' early-stage study of lead drug

The FDA has instituted a partial clinical hold on Phase 1 clinical trials of Pieris Pharmaceuticals' (NASDAQ: PIRS ) lead candidate PRS-343 until the company conducts an additional in-use and compatibility study with various infusion materials under specific conditions aimed at confirmin...

PIRS - Pieris Pharmaceuticals Announces Partial Clinical Hold On PRS-343

FDA requested a confirmatory laboratory-based in-use and compatibility study before enrolling new patients Currently-enrolled patients may continue to receive PRS-343 In its telephonic communication, FDA did not cite any adverse events in connection with its request Company ...

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