Söndag 11 Maj | 22:20:23 Europe / Stockholm

Bifogade filer

Kalender

Est. tid*
2026-02-13 08:20 Bokslutskommuniké 2025
2025-11-14 08:20 Kvartalsrapport 2025-Q3
2025-08-29 08:20 Kvartalsrapport 2025-Q2
2025-05-16 N/A X-dag ordinarie utdelning ELIC 0.00 SEK
2025-05-15 N/A Årsstämma
2025-05-15 08:20 Kvartalsrapport 2025-Q1
2025-02-03 - Bokslutskommuniké 2024
2024-11-28 - Kvartalsrapport 2024-Q3
2024-08-29 - Kvartalsrapport 2024-Q2
2024-05-27 - Kvartalsrapport 2024-Q1
2024-05-17 - X-dag ordinarie utdelning ELIC 0.00 SEK
2024-05-16 - Årsstämma
2024-02-20 - Extra Bolagsstämma 2024
2024-02-13 - Bokslutskommuniké 2023
2023-11-14 - Kvartalsrapport 2023-Q3
2023-08-29 - Kvartalsrapport 2023-Q2
2023-05-17 - X-dag ordinarie utdelning ELIC 0.00 SEK
2023-05-16 - Årsstämma
2023-05-16 - Kvartalsrapport 2023-Q1
2023-02-17 - Bokslutskommuniké 2022
2022-11-18 - Kvartalsrapport 2022-Q3
2022-08-22 - Kvartalsrapport 2022-Q2
2022-04-26 - Kvartalsrapport 2022-Q1
2022-03-08 - X-dag ordinarie utdelning ELIC 0.00 SEK
2022-03-07 - Årsstämma
2022-02-17 - Bokslutskommuniké 2021
2021-11-18 - Kvartalsrapport 2021-Q3
2021-08-20 - Kvartalsrapport 2021-Q2
2021-05-07 - X-dag ordinarie utdelning ELIC 0.00 SEK
2021-04-26 - Årsstämma
2021-04-14 - Kvartalsrapport 2021-Q1
2021-02-18 - Bokslutskommuniké 2020

Beskrivning

LandSverige
ListaFirst North Stockholm
SektorHälsovård
IndustriBioteknik
Elicera Therapeutics är verksamt inom läkemedelsbranschen. Bolaget är specialiserat inom forskning och utveckling inom immun-onkologi för cell- och genterapier för immunbaserad cancerbehandling. Utöver huvudverksamheten erbjuds även service och tillhörande kringtjänster. Verksamheten bedrivs med störst närvaro inom Sverige. Elicera Therapeutics har sitt huvudkontor i Göteborg.
2023-01-23 16:01:43

Gothenburg, January 23, 2022 - Elicera Therapeutics AB (publ) ("Elicera"), a clinical stage cell and gene therapy company developing next-generation therapies based on oncolytic viruses and CAR T-cells armed with the company's proprietary and commercially available platform iTANK, today announced that the Data Safety and Monitoring Board (DSMB) completed its third assessment of the ongoing clinical phase I/IIa study with oncolytic virus, ELC-100, in neuroendocrine tumors and recommended continuation of the trial, as planned.

The dose escalation study, which is carried out in collaboration with Uppsala University as sponsor, has previously been able to report signals of clinical activity in two of eight evaluable patients in the ELC-100 study, where a total of 12 patients are planned to be treated in four dose levels/cohorts. After the DSMB's recommendation to continue the trial, recruitment of the remaining three patients in the last cohort can commence.

About the ELC-100 clinical phase I/IIa dose escalation study

The ELC-100 study is conducted in two phases. Phase I, which is now underway, has the primary goal of investigating the safety of the treatment and determining the maximum tolerable dose. The first phase of the study has four dose levels with three patients at each level. In addition to determining the maximum tolerable dose, efficacy is also evaluated for example in the form of tumor response.

So far, no dose-limiting adverse events have been reported. Full efficacy reporting from the ELC-100 study is expected when the study is fully completed.

About ELC-100

ELC-100 is an oncolytic virus based on a genetically modified adenovirus that has been optimized for its ability to selectively enter and replicate in neuroendocrine cancer cells but not healthy cells. Tumor cell death is achieved via so-called oncolysis when the virus particles have replicated to a sufficient extent in the tumor cell that it explodes and dies. ELC-100 is currently being used in an ongoing phase I/IIa clinical trial in the treatment of neuroendocrine tumors.