Some RNS history. Sounded great at the time..but?25 Nov 2020 12:38
Have gone through a number of RNS's from since I first invested. Dates/reason for RNS below and some of the comments made by the company which have not been wholly accurate in hindsight. Interesting and dissapointing at the same time.
10th October 2018 New England Biolabs Affimer reagent licensing deal.
Avacta will receive a royalty on product sales, which may occur as soon as 2019.
10th December 2018. LG Chem Deal.
the Group expects to advance its lead programme, a PD-L1/LAG3 bispecific, into the clinic in 2020.
21st January 2019 Business Update
Multiple further licensing deals expected through 2019. I look forward to updating the market on progress during 2019 which I expect to be a year of very significant progress for the Company."
9th April 2019 Interims
First-time-in-human data is a significant value inflection point for the technology and a major de-risking point from a deal making perspective. The Group remains on track, to a tight schedule, to dose first patients in late 2020.
3 June 2019 TMAC Programme Accelerates
Key linker element of Avacta's novel TMACTM drug conjugate to be tested in humans within 12 months.
Avacta Group plc (AIM: AVCT), the developer of Affimer® biotherapeutics and research reagents, announces that it is planning to submit an IND/CTA application early in 2020 to test the TMAC linker in a phase I study in patients with selected solid tumours.
In an acceleration of the TMAC programme, Avacta is now in a position to test this critical TMAC linker in humans, a major de-risking milestone for the programme, early in 2020 and well ahead of its original plan.
18 October 2019 Interims
Acceleration of Tufts collaboration with planned regulatory submission in the first quarter of 2020.
7 diagnostics evaluations including 4 with top 10 global in vitro diagnostic companies all of which could lead to licensing deals.
14 projects with pharma and biotech companies including 4 out of the top 10 large pharma.
2 evaluations with bioprocessing companies, one being a global leader in affinity purification, and both with the potential to deliver licensing deals.
AVA6000 pro-Doxorubicin that is based on the Tufts technology, we have seen a dramatic improvement in safety in pre-clinical animal models. If we see a similar reduction in cardiotoxicity in humans in the planned phase I clinical trial of AVA6000 in 2020
23 Jan 2020 Trading Update
We are also due to take our first drug AVA6000, a re-engineered form of the chemotherapy Doxorubicin into the clinic in the middle of 2020, making it a ground-breaking yearfor the Group. The initial readout, which aims to show that the side effects of this chemotherapy have been reduced, are expected before the end of the year.
2nd April 2020 £2m Placing
Avacta will file a CTA application as soon as possible for a phase I dose escalation study for its lead preCISION pro-drug chemotherapy AVA6000 pro-doxorubicin.
From here came the Covid Rapid