Lördag 26 April | 16:09:27 Europe / Stockholm

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Est. tid*
2025-11-19 07:00 Kvartalsrapport 2025-Q3
2025-08-21 07:00 Kvartalsrapport 2025-Q2
2025-05-16 N/A X-dag ordinarie utdelning CANTA 0.00 SEK
2025-05-15 N/A Årsstämma
2025-05-13 07:00 Kvartalsrapport 2025-Q1
2025-02-21 - Bokslutskommuniké 2024
2024-12-02 - Extra Bolagsstämma 2025
2024-11-15 - Kvartalsrapport 2024-Q3
2024-08-28 - Kvartalsrapport 2024-Q2
2024-05-24 - X-dag ordinarie utdelning CANTA 0.00 SEK
2024-05-23 - Årsstämma
2024-05-21 - Kvartalsrapport 2024-Q1
2024-02-22 - Bokslutskommuniké 2023
2023-11-10 - Kvartalsrapport 2023-Q3
2023-08-22 - Kvartalsrapport 2023-Q2
2023-05-24 - X-dag ordinarie utdelning CANTA 0.00 SEK
2023-05-23 - Årsstämma
2023-05-23 - Kvartalsrapport 2023-Q1
2023-02-23 - Bokslutskommuniké 2022
2022-11-10 - Kvartalsrapport 2022-Q3
2022-08-30 - Kvartalsrapport 2022-Q2
2022-07-21 - Extra Bolagsstämma 2022
2022-05-24 - X-dag ordinarie utdelning CANTA 0.00 SEK
2022-05-23 - Årsstämma
2022-05-23 - Kvartalsrapport 2022-Q1
2022-02-24 - Bokslutskommuniké 2021
2021-11-11 - Kvartalsrapport 2021-Q3
2021-08-19 - Kvartalsrapport 2021-Q2
2021-05-27 - X-dag ordinarie utdelning CANTA 0.00 SEK
2021-05-26 - Årsstämma
2021-05-26 - Kvartalsrapport 2021-Q1
2021-02-25 - Bokslutskommuniké 2020
2020-11-12 - Kvartalsrapport 2020-Q3
2020-10-13 - Extra Bolagsstämma 2020
2020-08-20 - Kvartalsrapport 2020-Q2
2020-05-28 - X-dag ordinarie utdelning CANTA 0.00 SEK
2020-05-27 - Årsstämma
2020-05-27 - Kvartalsrapport 2020-Q1
2020-02-27 - Bokslutskommuniké 2019
2019-11-15 - Kvartalsrapport 2019-Q3
2019-08-22 - Kvartalsrapport 2019-Q2
2019-05-28 - X-dag ordinarie utdelning CANTA 0.00 SEK
2019-05-27 - Årsstämma
2019-05-27 - Kvartalsrapport 2019-Q1
2019-02-27 - Bokslutskommuniké 2018
2018-11-15 - Kvartalsrapport 2018-Q3
2018-08-21 - Kvartalsrapport 2018-Q2
2018-06-01 - X-dag ordinarie utdelning CANTA 0.00 SEK
2018-05-31 - Årsstämma
2018-05-15 - Kvartalsrapport 2018-Q1
2018-02-28 - Bokslutskommuniké 2017
2017-11-15 - Kvartalsrapport 2017-Q3
2017-08-23 - Kvartalsrapport 2017-Q2
2017-05-31 - X-dag ordinarie utdelning CANTA 0.00 SEK
2017-05-30 - Årsstämma
2017-05-15 - Kvartalsrapport 2017-Q1
2017-03-15 - Bokslutskommuniké 2016
2017-01-16 - Extra Bolagsstämma 2017
2016-11-21 - Kvartalsrapport 2016-Q3
2016-08-24 - Kvartalsrapport 2016-Q2
2016-05-25 - Årsstämma
2016-05-16 - Kvartalsrapport 2016-Q1
2016-03-02 - X-dag ordinarie utdelning CANTA 0.00 SEK
2016-03-01 - Bokslutskommuniké 2015
2015-11-17 - Kvartalsrapport 2015-Q3
2015-08-25 - Kvartalsrapport 2015-Q2
2015-05-19 - Kvartalsrapport 2015-Q1
2015-03-03 - Bokslutskommuniké 2014

Beskrivning

LandSverige
ListaSmall Cap Stockholm
SektorHälsovård
IndustriBioteknik
Cantargia är verksamt inom läkemedelsbranschen och fokuserar på utveckling av behandlingar för cancer och inflammatoriska sjukdomar. Bolaget forskar på nya terapier som kan förbättra patientresultat och livskvalitet. Verksamheten är global med en huvudsaklig närvaro i Europa och Nordamerika. Cantargia grundades 2009 och har sitt huvudkontor i Lund.
2025-04-25 19:00:00
  • Clinical findings show association between nadunolimab and lower incidence and later onset of CIPN
  • Preclinical data show prevention of both chemotherapy- and antibody-drug conjugate- (ADC) payload-induced neuropathy by a nadunolimab surrogate, supporting the clinical observations and suggesting an extension of benefits into the ADC field

Cantargia (Cantargia AB (publ); Nasdaq Stockholm: CANTA) today released a poster on nadunolimab’s potential in reducing the treatment-limiting burden of CIPN in metastatic cancer patients. Findings from the CANFOUR trial demonstrated that any-grade CIPN was less frequent in patients receiving higher doses of nadunolimab, compared to patients in the lower dose group. This is now supported by data from patients in two additional clinical trials as well as data from several preclinical models. Together the data suggests that nadunolimab may combine antitumor activity with a potent reduction of CIPN.

“The data that is presented at AACR show an association of nadunolimab with both a lower incidence and a delayed onset of CIPN caused by nab-paclitaxel or oxaliplatin. Given the persistent and often treatment-limiting nature of CIPN, any reduction in its severity or occurrence could represent a very meaningful clinical advantage. It is also very encouraging to see that a murine surrogate to nadunolimab can reduce not only CIPN induced by several different chemotherapy drugs, but also neuropathy induced by ADC payloads” said David Liberg, Chief Scientific Officer at Cantargia.

Peripheral neuropathic pain, a common and often severe side effect, can be triggered by both chemotherapy and ADCs through inflammatory pathways. This type of pain can profoundly impact a patient’s quality of life, sometimes necessitating dose reductions or even discontinuation of treatment.

Nadunolimab shows promising clinical benefit in combination with standard of care chemotherapies. The CANFOUR trial in advanced pancreatic cancer (PDAC) where nadunolimab was combined with nab-paclitaxel and gemcitabine, showed an impressive 48% ORR, 14.2 months OS, and 35% 24 months survival in patients with high levels of IL1RAP protein expression in tumor cells. Additionally, a potential neuroprotective role of nadunolimab was observed in the same trial, which could provide patients with dual benefits of tumor control and reduced treatment-related neuropathy.

In line with the data in the CANFOUR trial, analysis of data in the CESTAFOUR (nadunolimab in combination with FOLFOX) and CAPAFOUR (nadunolimab in combination with mFOLFIRINOX) trials in advanced solid tumor indications further supports nadunolimab’s potential neuroprotective role. In both clinical trials, an association between higher doses of nadunolimab and lower incidence and later onset of CIPN was observed. Furthermore, preclinical data showed that a mouse-specific nadunolimab surrogate antibody prevented neuropathy induced by the chemotherapeutic agents nab-paclitaxel, gemcitabine, vincristine, as well as the combination of nab-paclitaxel and gemcitabine. Additionally, chemotherapy was shown to induce upregulation of IL-1 family cytokines, providing mechanistic insight into the suggested role of nadunolimab in counteracting CIPN. Using a preclinical model, the IL1RAP surrogate could also prevent neuropathy caused by tubulin targeting ADC payloads. These findings support the hypothesis that nadunolimab may help mitigate neuroinflammation and protect against peripheral nerve damage caused by ADCs, a rapidly growing and effective class of therapeutics in clinical use, yet frequently limited by significant side effects such as peripheral neuropathy.

The preclinical studies were performed in collaboration with Dr. Hana Starobova and colleagues at the University of Queensland, Australia. Details of the poster are given below:

Poster number: 309
Poster title: Adding nadunolimab to chemotherapy or antibody drug-conjugates (ADCs) may improve antitumor efficacy and counteract peripheral neuropathy
Session date: April 27, 2025

The poster will be presented at the AACR annual meeting 2025 in Chicago, IL on April 27 from local time 2-5pm by Dr. Elin Jaensson Gyllenbäck from Cantargia. The poster will be uploaded on Cantargia’s webpage www.cantargia.com.