Connect Biopharma Reports First Half 2022 Financial Results and Provides Business Update
13 Setembro 2022 - 5:05PM
Connect Biopharma Holdings Limited (Nasdaq: CNTB) (Connect
Biopharma or the Company), a global, clinical-stage
biopharmaceutical company developing T cell-driven therapies to
treat inflammatory diseases, today announced financial results for
the six-month period ended June 30 and recent corporate highlights.
“2022 has been a dynamic year for Connect Biopharma so far, with
clinical progress in all three of our drug candidates, CBP-201, in
atopic dermatitis (AD) (Global Phase 2b trial), CBP-307 (Phase 2),
in ulcerative colitis (UC), and recently announced positive data
for our third candidate, CBP-174, in pruritus, each of which has
the potential to address large patient populations with persistent
unmet medical needs,” said Zheng Wei, Ph.D., Co-founder and CEO of
Connect Biopharma.
“With respect to our lead drug candidate, CBP-201, based on
recent feedback from China’s Center for Drug Evaluation (CDE) on
the CBP-201 China pivotal AD trial, we expect to report top-line
data from the stage 1, 16-week treatment period, in October, which
is earlier than we had anticipated. With these data, we plan to
initiate discussions with the CDE which, if positive, could result
in a New Drug Application (NDA) filing as early as 2024 for
commercial launch in China. We remain confident that ongoing and
future studies will continue to demonstrate the therapeutic
potential of CBP-201 with a convenient dosing schedule for patients
with AD as well as for other inflammatory-mediated diseases. To
that end, we anticipate, by the end of this year, initiating our
global CBP-201 Phase 3 trial in AD and in the first half of 2023,
completing enrollment in the CBP-201 global Phase 2 trial in
asthma,” concluded Dr. Zheng.
First Half 2022
Highlights
- Announced the top-line data from a global Phase 2b clinical
trial evaluating CBP-201 in patients with moderate-to-severe AD, in
which CBP-201 met all primary and key secondary efficacy
endpoints, with favorable safety data.
- Completed enrollment in a China pivotal study evaluating
CBP-201 in patients with moderate-to-severe AD.
- Completed an end of Phase 2 meeting with the U.S. Food and Drug
Administration (FDA) prior to the planned initiation of a global
Phase 3 clinical program to evaluate CBP-201 in patients with
moderate-to-severe AD.
- Announced the top-line data from a global Phase 2 clinical
trial evaluating CBP-307 in patients with UC, in which a key
secondary efficacy endpoint of Clinical Remission in Adapted Mayo
score was met.
- Named Chin Lee, M.D., MPH, Chief Medical Officer. Dr. Lee’s 15+
year career includes extensive experience in inflammation and
immunology drug development and spans key roles at companies
including Theravance, Genentech, Eli Lilly and Abbott.
Completed and Anticipated Upcoming
Milestones
- CBP-201 in AD:
- China pivotal trial: On track to report top-line primary
analysis data in October
- On track to initiate a global Phase 3 trial by the end of
2022
- CBP-201 in Asthma: Anticipate completing
enrollment in the global Phase 2 trial in the first half of 2023
and reporting its top-line results in the second half of 2023, both
timelines delayed approximately six months due to enrollment
challenges from the pandemic and the war in Ukraine.
- CBP-307 in UC: On track to complete Phase 2
maintenance phase by the end of 2022. The Company believes the
top-line results at 12 weeks warrant further clinical development
and is exploring strategic partnerships to progress CBP-307 into
future trials
- CBP-174 in Pruritus: Reported the successful
completion of the Phase 1 single ascending dose trial on August 30
in which CBP-174 was observed to be safe and well-tolerated with no
serious adverse events and no dose-limiting toxicities
identified
First Half 2022
Financial
Results
- Cash, cash equivalents, and short-term and long-term
investments were RMB 1,429.1 million (USD 212.9 million) as of June
30, 2022, compared to RMB 1,706.9 million as of December 31, 2021.
The decrease was mainly due to ongoing research and development
(R&D) and administrative costs associated with the Company’s
clinical drug programs. The Company believes it has sufficient cash
and investments to support planned operations into at least 2024
based on its current operating plans. Short-term and long-term
investments are indicated as Investments: Financial Assets at Fair
Value Through Other Comprehensive Income in the balance sheet.
- R&D expenses increased to RMB 340.8 million (USD 50.8
million) for the six months ended June 30, 2022, from RMB 217.8
million for the six months ended June 30, 2021. This increase was
driven primarily by higher clinical trial-related expenses for
CBP-201, including expenses related to advancing CBP-201 for AD in
China, and ongoing global Phase 2 trial costs for CBP-201 in
asthma, and global Phase 2 trial costs for CBP-307 in UC, as well
as higher personnel costs for additional R&D headcount.
- Administrative expenses increased to RMB 71.8 million (USD 10.7
million) for the six months ended June 30, 2022, compared with RMB
48.0 million for the six months ended June 30, 2021. The increase
was primarily due to higher personnel costs, including stock-based
compensation expenses, higher professional services costs, and
other costs associated with building out a public-company
infrastructure and supporting clinical trials.
- Net loss totaled RMB 401.3 million (USD 59.8 million) for the
six months ended June 30, 2022, compared with a net loss of RMB
942.5 million for the six months ended June 30, 2021. The net loss
in in the prior year period was higher due to the recognition of
RMB 674.3 million of fair value adjustments on preferred stock,
which was converted to common stock in last year’s IPO.
Conference Call and Webcast DetailsTo
participate in today’s conference call or webcast, at 4:30 p.m.
EDT/1:30 p.m. PDT today, please follow these options:
- To listen to the live webcast of the conference call, or the
replay, which will be available for 12 months, investors can follow
this link: https://edge.media-server.com/mmc/p/vftshcme.
- To participate in the live telephone conference call, follow
this link to register in advance: Registration Link for
Teleconference Dial In. Upon registering, a dial-in number and
unique PIN will be generated and is required to join the
conference call.
About Connect Biopharma Holdings LimitedConnect
Biopharma is a U.S. and China-based clinical-stage
biopharmaceutical company dedicated to improving the lives of
patients with inflammatory diseases through the development of
therapies derived from T cell research. The Company is building a
rich pipeline of proprietary small molecules and antibodies, using
functional T cell assays, to screen and discover potent product
candidates against validated immune targets. The Company’s lead
product candidate, CBP-201, is an antibody designed to target
interleukin-4 receptor alpha (IL-4Rα) in development for the
treatment of atopic dermatitis and asthma. The Company’s second
most advanced product candidate, CBP-307, is a modulator of S1P1 T
cell receptor and is in development for the treatment of ulcerative
colitis (UC). The Company’s third product candidate, CBP-174, is a
peripherally acting antagonist of histamine receptor 3, for the
treatment of pruritus associated with AD. For more information,
please visit: https://www.connectbiopharm.com/.
Forward-Looking StatementsConnect Biopharma
cautions that statements included in this press release that are
not a description of historical facts are forward-looking
statements. Words such as “may,” “could,” “will,” “would,”
“should,” “expect,” “plan,” “anticipate,” “believe,” “estimate,”
“intend,” “predict,” “seek,” “contemplate,” “potential,” “continue”
or “project” or the negative of these terms or other comparable
terminology are intended to identify forward-looking statements.
These statements include the Company’s plans to advance the
development of its product candidates, the timing of achieving any
development or regulatory milestones, and the potential of such
product candidates, including to achieve any benefit or profile or
any product approval, as well as the ability of its current cash
and investments position to support planned operations. The
inclusion of forward-looking statements should not be regarded as a
representation by Connect Biopharma that any of its plans will be
achieved. Actual results may differ materially from those set forth
in this release due to the risks and uncertainties inherent in the
Company’s business and other risks described in the Company’s
filings with the Securities and Exchange Commission (SEC),
including the Company’s Annual Report on Form 20-F filed with the
SEC on March 31, 2022, and its other reports. Investors are
cautioned not to place undue reliance on these forward-looking
statements, which speak only as of the date hereof, and Connect
Biopharma undertakes no obligation to revise or update this news
release to reflect events or circumstances after the date hereof.
Further information regarding these and other risks is included in
Connect Biopharma’s filings with the SEC which are available from
the SEC’s website (www.sec.gov) and on Connect Biopharma’s website
(www.connectbiopharm.com) under the heading “Investors.” All
forward-looking statements are qualified in their entirety by this
cautionary statement. This caution is made under the safe harbor
provisions of Section 21E of the Private Securities Litigation
Reform Act of 1995.
|
|
CONNECT BIOPHARMA HOLDINGS
LIMITEDUnaudited Interim Condensed Consolidated
Statements of Loss |
|
|
|
|
For Six Months Ended June 30, |
|
|
2021 |
|
2022 |
|
2022 |
|
|
RMB’000 |
|
RMB’000 |
|
USD’000(1) |
|
|
|
|
|
|
|
Research and development expenses |
|
(217,806 |
) |
|
(340,775 |
) |
|
(50,776 |
) |
Administrative expenses |
|
(47,965 |
) |
|
(71,830 |
) |
|
(10,703 |
) |
Other income |
|
5,041 |
|
|
1,584 |
|
|
236 |
|
Other (losses)/gains -
net |
|
(7,640 |
) |
|
9,241 |
|
|
1,378 |
|
Operating
loss |
|
(268,370 |
) |
|
(401,780 |
) |
|
(59,865 |
) |
|
|
|
|
|
|
|
Finance income |
|
180 |
|
|
1,294 |
|
|
193 |
|
Finance cost |
|
(22 |
) |
|
(58 |
) |
|
(9 |
) |
Finance income - net |
|
158 |
|
|
1,236 |
|
|
184 |
|
Fair value loss of financial
instruments with preferred rights |
|
(674,269 |
) |
|
- |
|
|
- |
|
Loss before income
tax |
|
(942,481 |
) |
|
(400,544 |
) |
|
(59,681 |
) |
Income tax expense |
|
- |
|
|
(737 |
) |
|
(110 |
) |
Loss |
|
(942,481 |
) |
|
(401,281 |
) |
|
(59,791 |
) |
|
|
|
|
|
|
|
Loss attributable
to: |
|
|
|
|
|
|
Owners of the Company |
|
(942,481 |
) |
|
(401,281 |
) |
|
(59,791 |
) |
|
|
|
|
|
|
|
|
|
|
Loss per
share |
|
|
|
|
|
|
|
|
|
|
|
RMB |
|
|
RMB |
|
|
USD |
|
Loss attributable to the
owners of the Company |
|
(942,481 |
) |
|
(401,281 |
) |
|
(59,791 |
) |
Weighted average number of
ordinary shares outstanding |
|
46,935,542 |
|
|
55,064,947 |
|
|
55,064,947 |
|
|
|
|
|
|
|
|
|
|
|
Basic and
diluted |
|
(20.1 |
) |
|
(7.3 |
) |
|
(1.1 |
) |
|
CONNECT BIOPHARMA HOLDINGS
LIMITEDUnaudited Interim Condensed Consolidated
Balance Sheets |
|
|
|
|
December 31, |
|
June 30, |
|
June 30, |
|
|
2021 |
|
2022 |
|
2022 |
|
|
RMB’000 |
|
RMB’000 |
|
USD’000(1) |
|
|
|
|
|
|
|
ASSETS |
|
|
|
|
|
|
|
|
|
|
|
|
|
Non-current
assets |
|
|
|
|
|
|
Property, plant and equipment |
|
59,337 |
|
|
66,700 |
|
|
9,938 |
|
Right-of-use assets |
|
22,821 |
|
|
25,354 |
|
|
3,778 |
|
Intangible assets |
|
560 |
|
|
529 |
|
|
79 |
|
Investments: |
|
|
|
|
|
|
|
|
|
Financial assets at fair value through other comprehensive
income |
|
- |
|
|
149,681 |
|
|
22,303 |
|
Other non-current assets |
|
18,806 |
|
|
5,606 |
|
|
835 |
|
Total non-current
assets |
|
101,524 |
|
|
247,870 |
|
|
36,933 |
|
|
|
|
|
|
|
|
Current
assets |
|
|
|
|
|
|
Cash and cash equivalents |
|
1,706,880 |
|
|
948,765 |
|
|
141,366 |
|
Other receivable and prepayments |
|
47,255 |
|
|
47,832 |
|
|
7,127 |
|
Investments: |
|
|
|
|
|
|
|
|
|
Financial assets at fair value through other comprehensive
income |
|
- |
|
|
330,673 |
|
|
49,270 |
|
Total current
assets |
|
1,754,135 |
|
|
1,327,270 |
|
|
197,763 |
|
Total
assets |
|
1,855,659 |
|
|
1,575,140 |
|
|
234,696 |
|
|
|
|
|
|
|
|
LIABILITIES |
|
|
|
|
|
|
Non-current
liabilities |
|
|
|
|
|
|
Lease liabilities |
|
163 |
|
|
2,248 |
|
|
335 |
|
Deferred income |
|
5,000 |
|
|
4,816 |
|
|
718 |
|
Total non-current
liabilities |
|
5,163 |
|
|
7,064 |
|
|
1,053 |
|
|
|
|
|
|
|
|
Current
liabilities |
|
|
|
|
|
|
Lease liabilities |
|
630 |
|
|
1,518 |
|
|
226 |
|
Trade payables |
|
81,195 |
|
|
101,627 |
|
|
15,142 |
|
Other payables and accruals |
|
32,840 |
|
|
35,441 |
|
|
5,281 |
|
Total current
liabilities |
|
114,665 |
|
|
138,586 |
|
|
20,649 |
|
Total
liabilities |
|
119,828 |
|
|
145,650 |
|
|
21,702 |
|
Net
assets |
|
1,735,831 |
|
|
1,429,490 |
|
|
212,994 |
|
|
|
|
|
|
|
|
SHAREHOLDERS’
EQUITY |
|
|
|
|
|
|
Share capital |
|
66 |
|
|
66 |
|
|
10 |
|
Share premium |
|
4,094,434 |
|
|
4,094,434 |
|
|
610,072 |
|
Treasury shares |
|
(1,164 |
) |
|
(1,164 |
) |
|
(173 |
) |
Share-based compensation reserve |
|
61,904 |
|
|
89,798 |
|
|
13,380 |
|
Other reserves |
|
(41,244 |
) |
|
25,802 |
|
|
3,843 |
|
Accumulated losses |
|
(2,378,165 |
) |
|
(2,779,446 |
) |
|
(414,138 |
) |
Total shareholders’
equity |
|
1,735,831 |
|
|
1,429,490 |
|
|
212,994 |
|
|
|
|
|
|
|
|
|
|
|
Total liabilities and
shareholders’ equity |
|
1,855,659 |
|
|
1,575,140 |
|
|
234,696 |
|
(1) |
Translations of the consolidated balance sheet and the consolidated
statement of loss from RMB into USD as of and for the six-month
period ended June 30, 2022, are solely for the convenience of the
readers and calculated at the rate of USD1.00=RMB 6.7114,
representing the exchange rate as of June 30, 2022, set forth in
the China Foreign Exchange Trade System. No representation is made
that the RMB amounts could have been, or could be, converted,
realized or settled into USD at that rate, or at any other rate, on
June 30, 2022, or any other date. |
|
|
|
|
INVESTOR and MEDIA CONTACT:Ina
McGuinness805.427.1372imcguinness@connectpharm.com
Corporate
Contacts:info@connectpharm.com
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