For research use only. We do not sell to patients.
← All classifications
Applications & RNA cargo

Ionizable lipids for in vivo T-cell engager

Ionizable lipids with product-specific evidence for in vivo delivery of RNA encoding T-cell engagers (TCEs / BiTEs). Compare the antibody target, RNA format, model and administration route for each lipid.

5 products currently listedResearch-use products only
Evidence noteTCEs redirect T cells by binding a target-cell antigen and CD3. Inclusion reflects the cited formulation and experiment; it does not establish direct T-cell delivery, clinical equivalence or product performance.
RNA-encoded T-cell engagers

CD19 · CLDN6 · B7H3

mRNA and self-amplifying RNA delivery

5 lipids · Intravenous evidence

View study references ↓
Browse this category

Browse the 5 selected lipids

5 products · 20 per page
Cat. No.Product NameField of ApplicationChemical Structure
Lipid 03-135Featured
Price on request

03-135 LNPs delivered mRNA encoding a CD19/CD3 T-cell engager and supported circulating antibody expression in mice.

CD19 × CD3 · mRNA · Intravenous

Study reference ↓
Lipid 03-135 chemical structure
Lipid 01-1Featured
Price on request

01-1 LNPs were used for CD19/CD3 T-cell engager expression and antitumor experiments in a human PBMC-engrafted Nalm6 leukemia model.

CD19 × CD3 · mRNA · Intravenous

Study reference ↓
Lipid 01-1 chemical structure
ALC-0366Featured

ALC-0366 is explicitly listed in the BNT142 formulation encoding the CLDN6/CD3 engager RiboMab02.1; the patent reports in vivo expression and pharmacokinetic studies.

CLDN6 × CD3 · mRNA (BNT142) · Intravenous

Study reference ↓
ALC-0366 chemical structure

IC8 LNPs delivered B7H3/CD3 BiTE-encoding mRNA, with in vivo antibody expression and antitumor experiments in mouse xenograft models.

B7H3 × CD3 · mRNA · Intravenous

Study reference ↓
IC-8(lipid MIC5) chemical structure
SM-102Featured

SM-102 LNPs delivered self-amplifying RNA encoding a CLDN6 nanobody-based T-cell engager, with circulating expression and antitumor studies in mice.

CLDN6 × CD3 · Self-amplifying RNA · Intravenous

Study reference ↓
SM-102 chemical structure

Evidence for category inclusion

Study-specific findings for research-use lipid selection.

DCL0008 · Lipid 03-135 — Patent evidence

03-135 LNPs delivered mRNA encoding a CD19/CD3 T-cell engager and supported circulating antibody expression in mice. Route: Intravenous.

WO2024131874A1, Example 7, paragraph [0362], Figure 3B.

DCL0009 · Lipid 01-1 — Patent evidence

01-1 LNPs were used for CD19/CD3 T-cell engager expression and antitumor experiments in a human PBMC-engrafted Nalm6 leukemia model. Route: Intravenous.

WO2024131874A1, Example 7, paragraphs [0362–0363], Figures 3B and 4A–4B.

DC60478 · ALC-0366 — Patent evidence

ALC-0366 is explicitly listed in the BNT142 formulation encoding the CLDN6/CD3 engager RiboMab02.1; the patent reports in vivo expression and pharmacokinetic studies. Route: Intravenous.

US20250009780A1, Table 2 (BNT142 composition), Figure 10 and the mouse / cynomolgus-monkey pharmacokinetic studies.

DC82301 · IC-8 (IC8; lipid MIC5) — Peer-reviewed study

IC8 LNPs delivered B7H3/CD3 BiTE-encoding mRNA, with in vivo antibody expression and antitumor experiments in mouse xenograft models. Route: Intravenous.

Huang et al. Advanced Science 10, 2205532 (2023); Results and Conclusion. DOI: 10.1002/advs.202205532.

DC52025 · SM-102 — Peer-reviewed study

SM-102 LNPs delivered self-amplifying RNA encoding a CLDN6 nanobody-based T-cell engager, with circulating expression and antitumor studies in mice. Route: Intravenous.

Zhu et al. Journal of Nanobiotechnology 24, 415 (2026); Figure 3 (SM-102 formulation), Figures 5–7 (in vivo studies). DOI: 10.1186/s12951-026-04319-z.

Each entry refers to the full RNA-LNP formulation in the cited study. These studies do not establish subcutaneous performance or guaranteed efficacy of the supplied lipid.