Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**TNFerade + 5-fluorouracil** is a combination regimen used primarily for the treatment of locally advanced pancreatic cancer. TNFerade Biologic (AdGVEGR.TNF.11D) is a replication-deficient adenoviral vector gene therapy designed to express human tumor necrosis factor-alpha (TNF-α) under the control of the Egr-1 promoter, which is activated by chemotherapy (such as 5-fluorouracil) and radiation. This gene therapy is administered directly into the tumor via endoscopic ultrasound (EUS) or percutaneous injection. The standard chemotherapy in this combination is **5-fluorouracil (5-FU)**, a classic antimetabolite cytotoxic agent that inhibits thymidylate synthase, blocking DNA synthesis and inducing apoptosis in rapidly dividing cells. The combination is typically administered alongside radiotherapy[1][2]. Trials have found this combination feasible and relatively safe, with the maximal tolerated dose for TNFerade Biologic defined as 4 × 10^11 particle units in combination with standard 5-FU and radiotherapy. TNFerade is developed by GenVec.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on TNFerade + 5-fluorouracil.