BioSenic SA: Information on the total number of voting rights and shares
01 März 2023 - 06:00PM
GlobeNewswire Inc.
BioSenic SA: Information on the total number of voting rights and
shares
REGULATED INFORMATION
Mont-Saint-Guibert, Belgium,
March
1st,
2023,
6.00pm
CEST – BIOSENIC (Euronext Brussels and
Paris: BIOS), the innovative company addressing unmet medical needs
in in the areas of innate immunity, inflammation and organ/function
repair, today announces an update in the total number of voting
rights and shares. The following information is published in
accordance with Article 15 of the Belgian Law of 2 May
2007 on the publication of major shareholdings in issuers whose
shares are admitted to trading on regulated market.
Total amount of share capital on 31 January 2023 |
EUR 33,800,669 |
Total number of shares with voting rights on 31 January 2023 |
124,008,857 |
Total number of shares admitted to listing on 31 January 2023 |
33,340,263 |
Total number of new shares issued between 01 February 2023 and 28
February 2023 |
0 |
Total amount of share capital on 28 February 2023 |
EUR 33,800,669 |
Total number of shares with voting rights on 28 February 2023 |
124,008,857 |
Total number of voting rights (denominator) on 28 February
2023 |
124,008,857 |
Total number of shares admitted to listing on 28 February 2023 |
124,008,857 (1) |
Total number of attributed warrants |
1,197,554 |
Total number of convertible bonds outstanding |
826 |
Total number of remaining CB commitments |
40 |
Total number of shares with voting rights that can be issued
following the exercise of the attributed warrants and CB
commitments, and the conversion of the convertible bonds |
21,550,767 (2) |
(1)
- 90,668,594 new shares issued to
Medsenic shareholders on 24 October 2022 (the "New
Shares") are listed as from 10 February 2023 but subject
to a lock-up until 24 July 2023 except for:
- 5% of the New Shares held by ABO
Securities released from the lock-up since 17 February 2023. These
New Shares were transferred by Medsenic shareholders to ABO
Securities Ltd as a final and definitive payment for their duties
as M&A advisor for the transaction.
- 2% of the New Shares held by each
of Véronique Pomi-Schneiter and François Rieger released from the
lock-up since 28 February 2023.
(2)
- 1,197,554 shares could be issued in
case all 1,197,554 attributed warrants were exercised.
- 285,714 shares could be issued in
case all 800 convertible bonds outstanding, issued in the private
placement on 6 May 2020, were converted into shares based on
the predetermined conversion price of EUR 7.00.
- 20,067,499 shares could be issued
in case all 40 CB commitments remaining and all 26 convertible
bonds outstanding of the ABO CB program signed on 30 May 2022 were
exercised and converted into shares based on the conversion price
of EUR 0.1644 (95% of the Volume-Weighted-Averaged-Price of
BioSenics’ shares on 27 February 2023).
About
BioSenic
BioSenic is a leading biotech company
specializing in the development of clinical assets issued from:
(i), the allogeneic cell therapy platform ALLOB and (ii) the
Arsenic TriOxide (ATO) platform. Key target indications for the
platforms include Graft versus Host Disease (GvHD), Systemic lupus
erythematosus (SLE), Systemic Sclerosis (SSc) and high-risk tibial
fractures.
Following the merger in October 2022, BioSenic
combines the strategic positionings and strengths of Medsenic and
Bone Therapeutics. The merger also enables Biosenic to add to its
innovative cell therapy platform and strong IP for tissue repair
protection with an entirely new arsenal of various
anti-inflammatory and anti-autoimmune formulations using the
immunomodulatory properties of ATO/OATO.
BioSenic is based in the Louvain-la-Neuve
Science Park in Mont-Saint-Guibert, Belgium. Further information is
available at http://www.biosenic.com.
About BioSenic technology
platforms
BioSenic’s technology is based on:
1) The allogeneic cell and gene
therapy platform, developed by Bone Therapeutics with
differentiated bone marrow sourced Mesenchymal Stromal Cells (MSCs)
that can be stored at the point of use in hospitals. Its current
investigational medicinal product, ALLOB, represents a unique,
proprietary approach to organ repair and specifically to bone
regeneration, by turning undifferentiated stromal cells from
healthy donors into bone-forming cells on the site of injury. These
cells are produced via a proprietary BioSenic scalable
manufacturing process. Following the CTA approval by regulatory
authorities in Europe, the Company has initiated patient
recruitment for the Phase IIb clinical trial with ALLOB in patients
with difficult tibial fractures, using its optimized production
process. ALLOB continues to be evaluated for other orthopedic
indications including spinal fusion, osteotomy, maxillofacial and
dental, and should be of value in new indications when cells will
be further adapted or transformed with additional targeting
properties.2) The Arsenic TriOxide (ATO) platform
developed by Medsenic. The immunomodulatory properties of ATO have
demonstrated a double basic effect on cells of the immune system.
The first effect is the increase of the cell oxidative stress in
activated B, T or other cells of the innate/adaptative immune
system to the point they will enter a cell death program
(apoptosis) and be eliminated. The second effect is potent
immunomodulatory properties on several pro-inflammatory cytokines
involved in inflammatory or autoimmune cell pathways. One direct
application is its use in onco-immunology to treat GvHD
(Graft-versus-Host Disease) in its chronic, established stage. GvHD
is one of the most common and clinically significant complications
affecting long-term survival of allogeneic hematopoietic stem cell
transplantation (allo-SCT). GvHD is primarily mediated by the
transplanted immune system that can lead to severe multiorgan
damage. Medsenic had been successful in a Phase II trial with its
intravenous formulation, allowing arsenic trioxide to be granted an
orphan drug designation status by FDA and EMA and is heading
towards an international Phase III confirmatory study, with a new,
IP protected, oral (OATO) formulation. Moderate to Severe forms of
Systemic Lupus erythematosus (SLE)° is another selected target,
using the same oral formulation. ATO has shown good safety and
significant clinical efficacy on several affected organs (skin,
mucosae and the gastro-intestinal tract) in a phase IIa study.
Systemic Sclerosis is, in addition, part of the clinical pipeline
of BioSenic. Preclinical studies on pertinent animal models are
positive. This gives good grounds to launch a Phase II clinical
protocol for this serious disease that badly affects skin, lungs or
vascularization, and with no actual current effective
treatment.
For further information, please
contact:
BioSenic SAFrançois Rieger,
PhD, Chief Executive OfficerTel: +33 (0)671 73 31
59investorrelations@biosenic.com
For Belgian Media and Investor
Enquiries:BepublicBert BouserieTel: +32 (0)488 40
44 77bert.bouserie@bepublicgroup.be
International Media Enquiries:IB
CommunicationsNeil Hunter / Michelle BoxallTel: +44 (0)20
8943 4685neil.hunter@ibcomms.agency / michelle@ibcomms.agency
For French Media and Investor
Enquiries:NewCap
MediaAnnie-Florence LoyerTel: +33 (0)1 44 71 00
12afloyer@newcap.fr
Certain statements, beliefs and opinions in this
press release are forward-looking, which reflect the Company or, as
appropriate, the Company directors’ current expectations and
projections about future events. By their nature, forward-looking
statements involve a number of risks, uncertainties and assumptions
that could cause actual results or events to differ materially from
those expressed or implied by the forward-looking statements. These
risks, uncertainties and assumptions could adversely affect the
outcome and financial effects of the plans and events described
herein. A multitude of factors including, but not limited to,
changes in demand, competition and technology, can cause actual
events, performance or results to differ significantly from any
anticipated development. Forward looking statements contained in
this press release regarding past trends or activities should not
be taken as a representation that such trends or activities will
continue in the future. As a result, the Company expressly
disclaims any obligation or undertaking to release any update or
revisions to any forward-looking statements in this press release
as a result of any change in expectations or any change in events,
conditions, assumptions or circumstances on which these
forward-looking statements are based. Neither the Company nor its
advisers or representatives nor any of its subsidiary undertakings
or any such person’s officers or employees guarantees that the
assumptions underlying such forward-looking statements are free
from errors nor does either accept any responsibility for the
future accuracy of the forward-looking statements contained in this
press release or the actual occurrence of the forecasted
developments. You should not place undue reliance on
forward-looking statements, which speak only as of the date of this
press release.
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