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Calendar

2024-11-13 Quarterly Report 2024-Q3
2024-08-21 Quarterly Report 2024-Q2
2024-05-15 Quarterly Report 2024-Q1
2024-03-28 Ex-date Ordinary Dividend CESSA 0.00 DKK
2024-03-27 Annual General meeting
2024-02-29 Year-end Report 2023
2023-11-16 Quarterly Report 2023-Q3
2023-08-24 Quarterly Report 2023-Q2
2023-05-12 Quarterly Report 2023-Q1
2023-03-24 Ex-date Ordinary Dividend CESSA 0.00 DKK
2023-03-23 Annual General meeting
2023-02-28 Year-end Report 2022
2022-11-18 Quarterly Report 2022-Q3
2022-11-04 Extra General Meeting 2022
2022-08-19 Quarterly Report 2022-Q2
2022-04-19 Quarterly Report 2022-Q1
2022-03-18 Ex-date Ordinary Dividend CESSA 0.00 DKK
2022-03-17 Annual General meeting
2022-02-24 Year-end Report 2021
2021-11-19 Quarterly Report 2021-Q3
2021-08-19 Quarterly Report 2021-Q2
2021-04-19 Quarterly Report 2021-Q1
2021-03-29 Ex-date Ordinary Dividend CESSA 0.00 DKK
2021-03-26 Annual General meeting
2021-02-11 Year-end Report 2020

Description

CountryDenmark
ListSpotlight DK
SectorHealth care
IndustryBiotechnology
Cessatech är verksamt inom läkemedelsbranschen. Bolaget är specialiserat inom forskning och utveckling av smärtstillande nässpray som vidare används för behandling av akuta smärttillstånd hos barn. Utöver huvudverksamheten erbjuds även tillhörande kringtjänster och relaterade produkter. Verksamheten drivs globalt med störst närvaro inom den nordiska marknaden. Huvudkontoret ligger i Köpenhamn.
2024-05-27 14:53:40
  • First patient has been dosed in Safety Study 0202 of lead candidate CT001.
  • The Safety Study 0202 is an open-label, prospective study to assess safety, tolerability, analgesic effect, and feasibility of CT001 in 150 paediatric patients with moderate to severe pain, in the emergency setting.
  • Cessatech expects the study to be completed by the end of 2024.

27 May - Cessatech A/S announces that the Safety Study 0202 has now been initiated with dosing of the first patient. The trial will assess safety, tolerability, analgesic effect, and feasibility of CT001 in 150 paediatric patients with moderate to severe pain, in the emergency setting.

The paediatric investigation plan (PIP) for CT001 nasal spray has been approved by the European Medicines Agency, and Safety Study 0202 is part of the clinical development plan for treatment of acute pain in children.

Comment from Jes Trygved, CEO of Cessatech
"We are very pleased with the initiation of this important and final trial for CT001, and the company is now moving into a different stage with last study - great work and effort by all the people involved in the preparation and initiation of this trial, including the countries and sites involved. CT001 is getting closer to the market and its potential patients and the period ahead will be extremely interesting".