6-K
BELITE BIO, INC (BLTE)
UNITEDSTATES
SECURITIESAND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OFFOREIGN PRIVATE ISSUER
PURSUANT TORULE 13a-16 OR 15d-16 UNDER
THE SECURITIESEXCHANGE ACT OF 1934
For the month of August 2023
Commission File Number: 001-41359
BeliteBio, Inc
(Exact name of registrant as specified in its charter)
Not Applicable
(Translation of registrant´s name into English)
12750 High Bluff Drive Suite 475,
San Diego, CA 92130
(Address of principal executive office)
Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.
Form 20-F x Form 40-F ¨
Indicate by check mark if the registrant is submitting this Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):
Yes ¨ No x
Indicate by check mark if the registrant is submitting this Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7):
Yes ¨ No x
Indicate by check mark whether the registrant by furnishing the information contained in this Form 6-K is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the Securities Exchange Act of 1934 Yes ¨ No x
On August 8, 2023, Belite Bio, Inc issued a press release entitled “ Belite Bio Reports Second Quarter 2023 Operational Highlights and Financial Results”. A copy of this press release is attached hereto as Exhibit 99.1 and is incorporated herein by reference.
This Report on Form 6-K shall be deemed to be incorporated by reference into all effective registration statements filed by the registrant under the Securities Act of 1933, and shall be a part thereof from the date on which this report is filed, to the extent not superseded by documents or reports subsequently filed or furnished.
EXHIBIT INDEX
SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
| Belite Bio, Inc | |
|---|---|
| By: | /s/ Yu-Hsin Lin |
| Name: | Yu-Hsin Lin |
| Title: | Chief Executive Officer and Chairman |
Date: August 8, 2023
Exhibit 99.1
Belite Bio Reports Second Quarter 2023 OperationalHighlights and Financial Results
| · | Completed enrollment in pivotal Phase 3 “DRAGON”<br>trial for Tinlarebant in adolescent Stargardt disease (“STGD1”) with 100 subjects enrolled across 11 countries worldwide |
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| · | First subject dosed with Tinlarebant in pivotal<br>global Phase 3 “PHOENIX” trial in Geographic Atrophy (“GA”) |
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| · | Oral, once-daily Tinlarebant continues to be<br>safe and well tolerated, slowing expansion of autofluorescence, reducing incident atrophic retinal lesion growth rate, and stabilizing<br>visual acuity up to 18-months in Phase 2 STGD1 trial (“LBS-008-CT02”) |
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| · | Strengthened balance sheet with $30 million<br>of gross proceeds from the underwritten public offering |
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| · | Final 2-year data of LBS-008-CT02 in STGD1<br>expected in Q4 2023 and interim Phase 3 safety and efficacy data from pivotal “DRAGON” trial expected in mid-2024 |
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| · | Conference Call and Webcast Wednesday, August<br>9, 2023, at 4:30 p.m. ET |
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SAN DIEGO, August 8, 2023- Belite Bio, Inc (NASDAQ: BLTE) (“Belite” or the “Company”), a clinical stage biopharmaceutical drug development company focused on advancing novel therapeutics targeting retinal degenerative eye diseases which have significant unmet medical needs, today announced its financial results for the three months ended June 30, 2023 and provided a general business update.
“We continue to execute on key milestones and make significant progress across our late-stage program for Tinlarebant, an oral, once-daily treatment for retinal degenerative diseases including STGD1 and GA,” said Dr. Tom Lin, Belite’s Chairman and CEO. “We are pleased to have dosed the first subject in our pivotal PHOENIX trial for GA, in addition to completing enrollment in the pivotal DRAGON trial in adolescent STGD1. We have several potential inflection points over the next 12-18 months and anticipate the final 2-year data of LBS-008-CT02 will become available during the fourth quarter of this year, and the interim Phase 3 safety and efficacy data from our pivotal DRAGON trial will become available in mid-2024.”
Dr. Nathan L. Mata, Chief Scientific Officer of Belite Bio added, “The slowing of lesion growth and stabilization of visual acuity up to 18-months in the Phase 2 STGD1 trial with Tinlarebant is encouraging and reinforces the potential to treat other retinal degenerative diseases like GA. Oral vitamin A based approaches like fenretinide have previously demonstrated promise for the treatment of GA, but were limited to only a subset of patients due to the poor bioavailability and potency of fenretinide. We believe the chemical design of Tinlarebant overcomes the limited potency and bioavailability associated with fenretinide and offers the potential for enhanced efficacy outcomes across a broader patient population with a more selective targeting for improved safety.”
Second Quarter 2023 Business Highlights and Upcoming Milestones:
Clinical Highlights
Tinlarebant (LBS-008) is designed to be an oral, potent, once-daily retinol binding protein 4 (RBP4) antagonist that decreases RBP4 levels in the blood and selectively lowers vitamin A (retinol) delivery to the eye without disrupting systemic retinol delivery to other tissues. Vitamin A is critical to normal vision but can accumulate as toxic byproducts leading to retinal cell death and vision loss diseases such as STGD1 and GA, the advanced form of dry Age-Related Macular Degeneration (dry AMD).
| · | Stargardt disease (STGD1): Accumulation<br>of cytotoxic bisretinoids has been implicated in the onset and progression of STGD1. Tinlarebant has been granted Fast Track and Rare<br>Pediatric Disease (RPD) designations by the U.S. Food and Drug Administration (FDA), and orphan drug designation (ODD) in the U.S. and<br>Europe for STGD1. There are currently no FDA-approved treatments for STGD1. |
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| o | LBS-008-CT02 trial: Ongoing, open-label, 2-year Phase 2 trial in adolescent STGD1 subjects |
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| § | 18-month efficacy and safety update (n = 12) at 2023 Association for Research<br>in Vision and Ophthalmology (ARVO) demonstrated: |
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| • | Tinlarebant continues to be safe and well tolerated |
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| • | Nearly 60% of subjects (7 out of 12) had no incident atrophic retinal lesions<br>as assessed by fundus autofluorescence (FAF) imaging |
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| • | Tinlarebant stabilized visual acuity with no significant loss and no clinically<br>significant changes in retinal thickness |
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| • | When compared with participants from the Prospective Cohort Study of Childhood-Onset<br>STGD1 by Georgiou et al., (2020), subjects in LBS-008-CT02 showed a reduced expansion of decreased autofluorescence (DAF) lesions from<br>baseline to 18 months (0.69 ± 0.72 mm^2^/year versus 0.28 ± 0.28 mm^2^/year, respectively)^(1)^.<br>Areas of DAF represent the combined area of questionably decreased autofluorescence (QDAF) + definitely decreased autofluorescence (DDAF)<br>lesions |
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| • | When compared with ProgStar study participants ≤ 18 years old with<br>only QDAF lesions at baseline, subjects in LBS-008-CT02 treated for up to 18 months showed^(1)^: |
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| - | Reduced expansion of DAF lesion size from baseline; |
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| - | Reduced expansion in DDAF lesion size from baseline |
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| o | Pivotal DRAGON trial: 2-year, randomized, double-masked, placebo-controlled, global, multi-center, pivotal Phase 3 trial in STGD1<br>subjects aged 12-20 years old: |
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| § | Enrollment complete, with 100 subjects across 11 countries worldwide including<br>sites in the U.S., the United Kingdom, Germany, Belgium, France, Switzerland, China, Hong Kong, Taiwan, Australia, and the Netherlands |
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| § | Primary efficacy endpoint is slowing of lesion growth rate; safety and tolerability<br>will also be assessed |
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| § | Mid 2024: Interim efficacy and safety data expected |
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| · | GeographicAtrophy (GA): GA, the advanced form of dry AMD, is a chronic degenerative disease of the retina that leads to blindness in the elderly.<br>Accumulation of toxic vitamin A byproducts (bisretinoids) has been implicated in the progression of GA. There are currently no FDA approved<br>orally administered treatments for GA. |
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| o | Pivotal PHOENIX Trial: 2-year prospective, randomized (2:1, active:placebo, n ~430), double-masked, placebo-controlled, global, multi-center,<br>Phase 3 trial in subjects with GA. |
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| § | Primary efficacy endpoint is slowing of lesion growth rate; safety and tolerability<br>will also be assessed |
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| § | First subject has been dosed |
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| § | Interim analysis expected at mid-point of the trial |
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Corporate Highlights
| · | Completed an underwritten public offering of American<br>Depositary Shares (“ADSs”) and warrants for gross proceeds of $30 million |
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| · | Hosted two key opinion leader (KOL) events in<br>May focused on a STGD1 disease overview and a discussion of Tinlarebant data in adolescent subjects: |
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| o | Professor Hendrik Scholl, M.D. (Chairman of the Department of Ophthalmology, University of Basel) who discussed STGD1 overview and<br>the 18-month data from the LBS-008-CT02 trial evaluating Tinlarebant for STGD1 |
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| o | Professor Michel Michaelides, M.D. (Professor of Ophthalmology at the UCL Institute of Ophthalmology) who discussed the progression<br>of childhood-onset STGD1 and the relevance of Tinlarebant’s LBS-008-CT02 trial 18-month data |
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Second Quarter 2023 Financial Results:
Cash and Cash Equivalents: As of June 30, 2023, the Company had $57.4 million in cash.
R&D Expenses:
For the three months ended June 30, 2023, research and development expenses were $5.5 million compared to $1.6 million for the same period in 2022. The increase resulted primarily from an increase in (x) expenses for conducting PHOENIX trial and (y) wages and salaries due to our R&D team expansion. For the six months ended June 30, 2023, research and development expenses were $11.2 million compared to $2.5 million for the same period in 2022. The increase in research and development expenses was primarily attributable to increases in (i) expenses related to conducting DRAGON and PHOENIX trials, and (ii) wages and salaries due to our R&D team expansion.
G&A Expenses:
For the three months ended June 30, 2023, general and administration expenses were $1.4 million compared to $0.9 million for the same period in 2022. The increase resulted primarily from an increase in (i) professional service fees and (ii) wages and salaries. For the six months ended June 30, 2023, general and administration expenses were $2.5 million compared to $1.1 million for the same period in 2022. The increase resulted primarily from an increase in (i) professional service fees and (ii) wages and salaries.
Net Loss:
For the three months ended June 30, 2023, the Company reported a net loss of $6.8 million or ($0.26) per share compared to $2.4 million or ($0.12) per share for the same period in 2022. For the six months ended June 30, 2023, the Company reported a net loss of $13.7 million or ($0.54) per share, compared to a net loss of $3.5 million or ($0.23) per share for the same period in 2022.
Webcast Information
Belite Bio will host a webcast to discuss the Company’s financial results and provide a business update. The call is scheduled on Wednesday, August 9, 2023, at 4:30 p.m. Eastern Time. To join the live webcast please click https://lifescievents.com/event/belitebio/. A replay will be available approximately two hours after the event for 90 days.
About Belite Bio
Belite Bio is a clinical stage biopharmaceutical drug development company focused on advancing novel therapeutics targeting retinal degenerative eye diseases with significant unmet medical needs, such as STGD1 and GA in advanced dry AMD, in addition to specific metabolic diseases. For more information, follow us on Twitter, Instagram, LinkedIn, Facebook or visit us at www.belitebio.com.
Important Cautions Regarding Forward Looking Statements
This press release contains forward-looking statements about futureexpectations, plans and prospects, as well as any other statements regarding matters that are not historical facts. These statements includebut are not limited to statements regarding the potential implications of clinical data for patients, clinical development, regulatorymilestones of its product candidates, and any other statements containing the words “expect”, “will”, “believe”, “target”, “anticipate”, and other similar expressions. Actual results may differ materially from those indicatedin the forward-looking statements as a result of various important factors, including but not limited to Belite Bio’s ability todemonstrate the safety and efficacy of its drug candidates; the clinical results for its drug candidates, which may not support furtherdevelopment or regulatory approval; expectations for the timing of initiation, enrollment and completion of, and data relating to, itsclinical trials; the content and timing of decisions made by the relevant regulatory authorities regarding regulatory approval of BeliteBio’s drug candidates; whether additional clinical trials may be required for DRAGON or PHOENIX studies based on their respectivedata; the potential efficacy of Tinlarebant, as well as those risks more fully discussed in the “Risk Factors” section inBelite Bio’s filings with the U.S. Securities and Exchange Commission. All forward-looking statements are based on information currentlyavailable to Belite Bio, and Belite Bio undertakes no obligation to publicly update or revise any forward-looking statements, whetheras a result of new information, future events or otherwise, except as may be required by law.
BELITE BIO, INC
UNAUDITED CONDENSED CONSOLIDATED STATEMENTSOF OPERATIONS AND COMPREHENSIVE LOSS
(Amounts in thousands of US Dollars, exceptshare and per share amounts)
| For the Three Months | For the Six Months | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ended June 30, | Ended June 30, | |||||||||||
| 2022 | 2023 | 2022 | 2023 | |||||||||
| Expenses | ||||||||||||
| Research and development | 1,579 | 5,516 | 2,457 | 11,239 | ||||||||
| General and administrative | 927 | 1,355 | 1,102 | 2,513 | ||||||||
| Total operating expenses | 2,506 | 6,871 | 3,559 | 13,752 | ||||||||
| Loss from operations | (2,506 | ) | (6,871 | ) | (3,559 | ) | (13,752 | ) | ||||
| Other income (expense): | ||||||||||||
| Total other income, net | 115 | 62 | 98 | 54 | ||||||||
| Loss before income tax | (2,391 | ) | (6,809 | ) | (3,461 | ) | (13,698 | ) | ||||
| Income tax expense | - | 3 | - | 9 | ||||||||
| Net loss | (2,391 | ) | (6,812 | ) | (3,461 | ) | (13,707 | ) | ||||
| Other comprehensive income (loss) | ||||||||||||
| Foreign currency translation adjustments, net of nil tax | (182 | ) | 76 | (157 | ) | (60 | ) | |||||
| Total comprehensive loss | (2,573 | ) | (6,888 | ) | (3,618 | ) | (13,767 | ) | ||||
| Weighted average number of ordinary shares used in per share calculation: | ||||||||||||
| - Basic and Diluted | 19,659,441 | 25,785,147 | 14,992,848 | 25,350,949 | ||||||||
| Net loss per ordinary share | ||||||||||||
| - Basic and Diluted | $ | (0.12 | ) | $ | (0.26 | ) | $ | (0.23 | ) | $ | (0.54 | ) |
BELITE BIO, INC
UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS
(Amounts in thousands of US Dollars, exceptshare amounts)
| December 31, | June 30, | |||
|---|---|---|---|---|
| 2022 | 2023 | |||
| Current assets | $ | 42,807 | $ | 59,137 |
| Other assets | 1,466 | 1,558 | ||
| TOTAL ASSETS | $ | 44,273 | $ | 60,695 |
| TOTAL LIABILITIES | $ | 2,772 | $ | 4,978 |
| TOTAL SHAREHOLDERS’ EQUITY | 41,501 | 55,717 | ||
| TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY | $ | 44,273 | $ | 60,695 |
| Ordinary shares authorized | 492,179,086 | 400,000,000 | ||
| Ordinary shares issued and outstanding | 24,898,908 | 27,229,255 |
Media and Investor Relations Contact:
Jennifer Wu /ir@belitebio.com
Tim McCarthy /tim@lifesciadvisors.com
Note: (1) Although we have compared the published data for the above studies to our interim data in the LBS-008-CT02 trial, the value of such comparisons is limited because they are derived from studies conducted under different protocols, at different sites, with different patient populations, and results were analyzed using non-standardized methods. We note our future trials may not confirm the comparisons or analyses we have made to date.
(2) For each subject, the mean lesion size between eyes was determined and the average value for the lesion sizes within each study group was calculated. The data show mean lesion sizes within each group ± standard error of the mean at each timepoint.