Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LTR192G + dscCfaE is an investigational recombinant protein subunit vaccine combination developed by the U.S. Army Medical Research and Development Command (USAMRDC) for the prevention of diarrhea caused by enterotoxigenic *Escherichia coli* (ETEC). The vaccine consists of two primary components: dscCfaE, a donor strand-complemented recombinant protein derived from the CfaE adhesin subunit of CFA/I fimbriae, and LTR192G, a detoxified single-mutant heat-labile enterotoxin (LT) that acts as a potent mucosal adjuvant. The vaccine is designed to elicit antibodies that block the adherence of ETEC to the intestinal epithelium, thereby preventing colonization and subsequent diarrheal disease. It has been evaluated in Phase 2 clinical trials using intradermal administration to assess efficacy against experimental challenge with ETEC strain H10407.
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 LTR192G + dscCfaE.