2 hours ago

Redeye views today's update from the MERECA as a positive and expected confirmation of previously reported results. We see no material

Med hela tre pågående kliniska studier inväntar rapportaktuella Immunicum nya resultat för huvudkandidaten ilixadencel. Bolaget med vd Carlo de Sousa i spetsen ser fram emot att under året ytterligare validera potentialen hos läkemedelskandidaten. Trots tydliga tecken på framsteg inom onkologifältet är cancer fortfarande högt på listan av sjukdomar som människor världen över 2020-12-31 Immunicum has received Orphan Drug Designation (ODD) from the U.S. Food and Drug Administration (FDA) for ilixadencel. Ilixadencel is a cell-based, off-the-shelf immune primer, for the treatment of Soft Tissue Sarcoma (STS).

During the trial, 88 patients were randomly assigned in a two-to-one ratio to the Immunicum AB (publ) Receives FDA Orphan Drug Designation for Ilixadencel as a Treatment for Hepatocellular Carcinoma (HCC) Immunicum AB (publ; IMMU.ST) announced today that it has received Orphan Drug Designation (ODD) from the U.S. Food and Drug Administration (FDA) for the Company’s lead candidate, ilixadencel, a cell-based, off-the-shelf immune primer, for the treatment of … 2020-05-06 For Immunicum, 2019 was a year of important clinical advancements with their lead candidate, ilixadencel. It demonstrated promising potential in both the MERECA and the GIST studies from which topline results were announced. These advancements were the main focus of the year-end report released last week. BioStock caught up with the company’s interim CEO, Alex […] In today’s Sunday Interview we talk to Carlos de Sousa, CEO of Immunicum. He shares his thoughts on why lead drug candidate ilixadencel may be the next generation of immuno-oncology therapies, on negotiating with two of the world’s biggest pharma companies and on what made some of Sweden’s top institutional investors, including hedge fund giant Max Mitteregger, commit […] Immunicum erhöll särläkemedelsstatus, Orphan Drug Designation, från FDA för ilixadencel för behandling av levercancer, specifikt hepatocellular carcinoma (HCC).

Immunicum AB (publ) erhåller särläkemedelsstatus, ODD, från EMA för ilixadencel för Börsen immunicum Immunicum: I fredags, efter börsens

➢ Ilixadencel beviljades ATMP-certiering från EMA gällande Immunicum kommer vid årets virtuella ESMO-kongress att presentera en del av prekliniska data relaterad till ilixadencel. Det framgår av ett pressmeddelande.

Feb 19 (Reuters) - Immunicum AB ::REG-IMMUNICUM AB (PUBL) RECEIVES ORPHAN DRUG DESIGNATION FROM EMA FOR ILIXADENCEL

With complementary therapeutic approaches in Phase II clinical development that are based on intratumoral priming and cancer relapse vaccination, the company aims to improve survival outcomes and quality of life for a broad Immunicum’s lead candidate, ilixadencel, just got a big boost in its development by being granted regenerative medicine advanced therapy designation by the FDA. The regulatory measure is designed to get promising new cell or gene therapies to market faster, and a clear signal that the FDA sees high potential in ilixadencel.

Yesterday, the company announced an update on the study that seems to indicate that their candidate is providing a survival benefit to patients.
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Ilixadencel is a cell-based, off-the-shelf immune primer, for the treatment of Soft Tissue Sarcoma (STS). New CEO shares vision for Immunicum. With such deal making experience, Sven Rohmann is a welcome addition to the Immunicum team as the company moves forward with ilixadencel in clinical trials and continues its plans for partnering. BioStock was able to get in touch with the new CEO and ask him about his plans for the company. 2 hours ago 2021-04-09 Immunicum AB (publ) today announced updated survival data from the Company’s randomized Phase II MERECA trial evaluating its off-the-shelf immune primer, ilixadencel, in combination with Immunicum AB (publ; IMMU.ST) tillkännager idag att bolaget har erhållit särläkemedelsstatus (Orphan Drug Designation, ODD) från den amerikanska läkemedelsmyndigheten, FDA, för bolagets ledande kandidat ilixadencel, en cellbaserad och lagringsbar immunaktiverare, för behandling av … EVELYN PESIKAN, ilixadencel, Immunicum, MERECA ATMP (Advanced Therapy Medicinal Products) är förkortningen för det många anser kommer att utgöra en viktig del i framtidens cancerläkemedel.

The company most recently presented comprehensive pre-clinical results showing that this transformation leads to an immunogenic shift. In May 2020, Immunicum received Regenerative Medicine Advanced Therapy designation from the FDA for ilixadencel for the treatment of patients with metastatic Renal Cell Carcinoma. In December 2020 , Immunicum announced that it received Fast Track Designation from the FDA for ilixadencel in Gastrointestinal Stromal Tumors (GIST) and Orphan Drug Designation by the FDA for ilixadencel in hepatocellular carcinomas.
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För patienter med huvud- och halscancer eller magcancer kombineras ilixadencel med avelumab (Bavencio®) som Immunicum får tillgång till

Immunicum AB (publ) today announced updated survival data from the Company’s randomized Phase II MERECA trial evaluating its off-the-shelf immune primer, ilixadencel, in combination with sunitinib Ilixadencel is an off-the-shelf cell-based cancer immunotherapy developed for the treatment of solid tumors. Its active ingredient is activated allogeneic dendritic cells, derived from healthy Ilixadencel is an off-the-shelf cell-based cancer immunotherapy developed for the treatment of solid tumors. Its active ingredient is activated allogeneic dendritic cells, derived from healthy Intratumoral administration of an immune primer is a therapeutic vaccine strategy aimed to trigger dendritic cell (DC)-mediated cross-presentation of cell-associated tumor antigens to cytotoxic CD8 + T cells without the need for tumor antigen characterization. Ilixadencel is an off-the-shelf cell-based cancer immunotherapy developed for the treatment of solid tumors.

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Immunicum AB (publ; IMMU.ST) announced today that it has received Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration (FDA) for the Company’s lead