BIOINVENT INTERNATIONAL AB - Clinical supply agreement with
AstraZeneca to support Phase 1/2a BI-1206 combination study - BI-1206 to be evaluated in combination with Calquence® and rituximab in Phase 1/2a trial in non-Hodgkin's lymphoma
- The ongoing rituximab combination trial will be expanded to include the triplet arm
Under the terms of the supply agreement,
"Having already shown the benefits of combining BI-1206 with rituximab, we believe the addition of Calquence for a triplet combination could further improve clinical outcomes for patients with non-Hodgkin's lymphoma, including follicular lymphoma and mantle cell lymphoma, " said Dr. Martin Welschof, CEO of
The Phase 1 part - intravenously (IV) administered BI-1206 - has been completed with impressive early signs of clinical efficacy. The Phase 2a IV dose expansion cohort is currently enrolling patients, and it will look to enroll patients to be treated with the triplet. A subcutaneous (SC) formulation is being developed in parallel to the IV and it is expected to bring a great deal of convenience to the treatment. The Calquence expansion cohort is expected to enroll approximately 30 patients at sites in
About BI-1206
BI-1206 is one of BioInvent’s most advanced drug candidates and is developed to re-establish the clinical effect of existing cancer treatments such as pembrolizumab and rituximab, drugs with combined global sales of approximately
The drug candidate is evaluated in two separate clinical programs, one for the treatment of non-Hodgkin’s lymphoma (NHL, a type of blood cancer) and one for the treatment of solid tumors. Two delivery formulations (intravenous (IV) and (subcutaneous (SC) of BI-1206 are being evaluated in parallel.
BI-1206 in NHL
All patients in the ongoing Phase 1/2a study have previously been treated with one or more rituximab containing treatments. Results from the intravenous (IV) Phase 1 part (dose escalation) showcase responses across the dose range of 30-100 mg, including 4 complete responders (CR), 3 partial responders (PR) and 4 cases of stable disease (SD) out of 15 evaluable patients. No maximum tolerated dose has been defined, and Phase 2a dose IV expansion cohort is currently enrolling patients.
Among the CR population, responses have been long-lasting, three of them lasting years after end of treatment, while the 4th is still on treatment. As of
In
About
The Company generates revenues from research collaborations and license agreements with multiple top-tier pharmaceutical companies, as well as from producing antibodies for third parties in the Company's fully integrated manufacturing unit. More information is available at www.bioinvent.com. Follow on the social media platform X: @BioInvent.
For further information, please contact:
Phone: +46 (0)46 286 85 50
Email: cecilia.hofvander@bioinvent.com
Co. Reg. No. Org nr: 556537-7263
Visiting address: Ideongatan 1
Mailing address: 223 70 LUND
Phone: +46 (0)46 286 85 50
www.bioinvent.com
The press release contains statements about the future, consisting of subjective assumptions and forecasts for future scenarios. Predictions for the future only apply as the date they are made and are, by their very nature, in the same way as research and development work in the biotech segment, associated with risk and uncertainty. With this in mind, the actual outcome may deviate significantly from the scenarios described in this press release. This press release is published in Swedish and English. In the event of any difference between the English version and the Swedish original, the Swedish version shall prevail. For a more detailed description of risk factors, see section “Risks and Risk Management,” page 47, in the Company’s annual report 2022.
© Modular Finance, source
