Pharma Pioneer

First Patient Treated in Phase 1b/2 Pancreatic Cancer Trial with AIM's Ampligen® and AstraZeneca's Imfinzi®

29 May 2024
2 min read

AIM ImmunoTech Inc., a biopharmaceutical firm listed on the NYSE American, has initiated a Phase 1b/2 clinical trial at Erasmus Medical Center for patients with advanced pancreatic cancer. The study, known as DURIPANC, combines the company's drug Ampligen® (rintatolimod) with Imfinzi® (durvalumab), an anti-PD-L1 immune checkpoint inhibitor from AstraZeneca, to explore the potential of this combination in treating the disease.
The primary goal of the Phase 1b is to assess the safety of the combined therapy, while the Phase 2 aims to evaluate its clinical efficacy. Prof. Casper H.J. van Eijck, a pancreatic surgeon at Erasmus MC, is optimistic about the trial's potential to improve outcomes for patients with metastatic pancreatic cancer and anticipates completing the initial phase within six months.
The trial plans to enroll a total of up to 43 participants. Treatment will begin with Ampligen administered intravenously at a dose of 200 mg twice weekly for six weeks, with the option to escalate to 400 mg. Following this, durvalumab will be introduced at a dose of 1500 mg every four weeks for a possible 48 weeks, subject to disease progression and tolerability.
AIM ImmunoTech specializes in developing therapeutics for cancer, immune disorders, and viral diseases, including COVID-19. Their flagship product, Ampligen, is a dsRNA and TLR3 agonist with demonstrated activity against various cancers and diseases in clinical trials.

How to obtain the latest research advancements in the field of biopharmaceuticals?

In the Synapse database, you can keep abreast of the latest research and development advances in drugs, targets, indications, organizations, etc., anywhere and anytime, on a daily or weekly basis. Click on the image below to embark on a brand new journey of drug discovery!

图形用户界面, 文本, 应用程序, 聊天或短信

描述已自动生成

Aulos Bioscience Shares Favorable Preliminary Phase 1/2 Data for AU-007 at 2024 ASCO Meeting
Latest Hotspot
4 min read
Aulos Bioscience Shares Favorable Preliminary Phase 1/2 Data for AU-007 at 2024 ASCO Meeting
29 May 2024
Aulos Bioscience revealed preliminary outcomes from its Phase 1/2 study of AU-007.
Read →
European Commission Approves Celltrion's Omlyclo®, First Omalizumab Biosimilar in Europe
Latest Hotspot
3 min read
European Commission Approves Celltrion's Omlyclo®, First Omalizumab Biosimilar in Europe
29 May 2024
Celltrion gains European Commission approval for Omlyclo® (CT-P39), the first omalizumab biosimilar sanctioned in Europe.
Read →
EMA Approves Henlius and Organon's Biosimilar HLX14 for Prolia® and Xgeva®
Latest Hotspot
3 min read
EMA Approves Henlius and Organon's Biosimilar HLX14 for Prolia® and Xgeva®
28 May 2024
The European Medicines Agency (EMA) has approved the filings by Henlius and Organon for their biosimilar candidate HLX14 to Prolia® and Xgeva® (denosumab).
Read →
Kymera Therapeutics Reveals New Preclinical Data for KT-621, an Oral STAT6 Degrader, at ATS Conference
Latest Hotspot
3 min read
Kymera Therapeutics Reveals New Preclinical Data for KT-621, an Oral STAT6 Degrader, at ATS Conference
28 May 2024
Kymera Therapeutics Unveils Novel Preclinical Findings for KT-621, an Oral STAT6 Degrader, at ATS Conference.
Read →
Get started for free today!
Accelerate Strategic R&D decision making with Synapse, PatSnap’s AI-powered Connected Innovation Intelligence Platform Built for Life Sciences Professionals.
Start your data trial now!
Synapse data is also accessible to external entities via APIs or data packages. Leverages most recent intelligence information, enabling fullest potential.