Destiny Pharma
plc
("Destiny Pharma" or "the
Company")
Cardiac surgery patients
treated with XF-73 Nasal gel require significantly fewer
post-surgical antibiotics
Further data from Phase 2b
study to be presented at ID Week, a leading US infectious disease
conference
Brighton, United
Kingdom - 22 July 2024 - Destiny Pharma (AIM: DEST), a clinical stage biotechnology
company focused on the development and
commercialisation of novel medicines to prevent and cure life
threatening infections, today announced that new clinical data from
its Phase 2b clinical trial on XF-73 in cardiac surgery patients
has been accepted for presentation at the ID Week conference, the
joint annual meeting of the Infectious
Diseases Society of America and the Society for Healthcare
Epidemiology of America on the 16-19 October 2024 in Los
Angeles, USA.
The title of the presentation is, 'Impact of Exeporfinium Chloride (XF-73) Nasal
Gel on the Use of Post-Operative Anti-staphylococcal Antibiotics in
Cardiovascular Surgery Patients: Results from a Randomised,
Placebo-Controlled Phase 2 Study.'
Previously, the Company reported on achieving
the primary endpoint for XF-73 Nasal gel, i.e. >99% reduction in
nasal S. aureus
compared to placebo one hour before open heart surgery, (p <
0.0001), Mangino et al.
20231.
Further planned data analysis of a secondary
endpoint within the clinical trial investigated the use by
physicians of post-surgical systemic antibiotics prescribed >48
hours after surgery. Significantly fewer patients in the XF-73
treatment arm received post-operative anti-staphylococcal
antibiotics: 46.5% (20 of a total population of 43), compared to
70% (28 of a total population of 40) in the placebo group, p=0.045,
which suggests that antibiotics may have been prescribed as an
early intervention in more patients in the placebo arm.
The observed reduction of the use of
post-operative antibiotics in the XF-73 arm is consistent with the
principles of good antimicrobial stewardship which are crucial for
managing and preventing infections more effectively and for
maintaining the efficacy of antibiotics, reducing healthcare
complications, and improving patient safety.
Additional advantages of the XF-73
Nasal gel include the short, 24 hour, pre-surgical dosing regimen,
rapidity of S. aureus
nasal decolonisation, remote likelihood of resistance emergence,
and the duration of effect. These features provide a good fit with
clinical practice, potentially enabling infection risk reduction
peri-operatively, enhancing flexibility for scheduling surgeries,
and augmenting antibiotic stewardship efforts. Phase 3 studies are
being planned to evaluate and gain regulatory approval for
XF-73.
XF-73 has also demonstrated efficacy against
the hospital superbug methicillin-resistant Staphylococcus aureus (MRSA). In
studies published last year XF-73 was potent against all 840 MRSA
strains collected from infected patients from 33 countries
worldwide (Rhys Williams et
al. 2023)2 and was shown to be up to 1000 times
more efficacious than nasal mupirocin (the most commonly used nasal
antibiotic) at treating MRSA in a skin infection model, (Zhang
et al.
2023)3.
Dr Debra
Barker, Interim Chief Medical Officer of Destiny Pharma,
said: "The
data to be presented at ID Week highlights the ability of XF-73
Nasal gel to significantly reduce the need for post-surgical
antibiotic use. With antimicrobial resistance continuing to present
an existential threat, these data highlight the value that XF-73
Nasal can provide in meeting this challenge while delivering
favourable patient outcomes."
References:
1. Mangino JE, Firstenberg
MS, Milewski RKC, et al., 2023. Exeporfinium chloride (XF-73) nasal
gel dosed over 24 hours prior to surgery significantly reduced
Staphylococcus aureus nasal carriage in cardiac surgery patients:
Safety and efficacy results from a randomized placebo-controlled
phase 2 study. Infection Control & Hospital Epidemiology,
2023;44(7):1171-1173. doi:10.1017/ice.2023.17
2. William Rhys-Williams,
Helen Marie Galvin and William Guy Love, 2023. Screening of the
novel antimicrobial drug, XF-73, against 2,527 Staphylococcus
species clinical isolates. Frontiers in Cellular and Infection
Microbiology, 2023; 13.
doi.org/10.3389/fcimb.2023.1264456
3. Zhang, C.,
Li, J., Lu, R., Wang, S., Fu, Z., & Yao, Z., 2023.
Efficacy of a Novel Antibacterial Agent Exeporfinium
Chloride, (XF-73), Against Antibiotic-Resistant Bacteria in Mouse
Superficial Skin Infection Models. Infection and Drug Resistance,
16, 4867-4879. doi.org/10.2147/IDR.S417231
For further
information, please contact:
Destiny Pharma
plc
Chris Tovey, CEO
Shaun Claydon, CFO
+44 (0)1273 704 440
pressoffice@destinypharma.com
FTI
Consulting
Ben Atwell / Simon Conway
+44 (0) 203 727 1000
destinypharma@fticonsulting.com
About Destiny
Pharma
Destiny Pharma is an innovative, clinical-stage
biotechnology company focused on the development and
commercialisation of novel medicines that can prevent
life-threatening infections. The Company's drug development
pipeline includes two late-stage assets XF-73 Nasal gel, a
proprietary drug targeting the prevention of post-surgical
staphylococcal hospital infections including MRSA and NTCD-M3, a
microbiome-based biotherapeutic for the prevention of C. difficile
infection (CDI) recurrence which is the leading cause of hospital
acquired infection in the US.
For further information on the company, please visit
www.destinypharma.com.
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