20220331-招银国际-Lemzoparlimab_showed_encouraging_data_on_MDS_4页_947kb
报告摘要
I-Mab BioPharma (IMAB US) Summary
Core Information
I-Mab BioPharma is a biotech company with a strong focus on oncology and other therapeutic areas. The company has a robust pipeline of drug candidates and is actively working on multiple assets for commercialization in the next three years. It also has a solid cash position and is addressing potential US delisting risks by accelerating its Hong Kong listing.
Financial Highlights
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Revenue (RMB mn):
- FY20A: 1,543
- FY21A: 88
- FY22E: 794
- FY23E: 1,270
- FY24E: 2,040
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Net Profit (RMB mn):
- FY20A: 471
- FY21A: (2,332)
- FY22E: (1,198)
- FY23E: (774)
- FY24E: (187)
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EPS (RMB per ADS):
- FY20A: 8.07
- FY21A: (30.69)
- FY22E: (14.99)
- FY23E: (9.68)
- FY24E: (2.34)
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Cash Position:
- As of end-2021: RMB4.3bn
- Expected to support future R&D activities and milestone payments
-
Target Price:
- US$103.60 (Maintained from previous estimate)
- Potential upside: +446.70% from current price of US$18.95
Key Developments
1. Lemzoparlimab (CD47) for MDS
- Phase 2 Trial: Over 70 patients with newly diagnosed MDS or AML have been dosed with leMZoparlimab in combination with AZA.
- Interim Results: For 22 MDS patients with a median treatment duration of ≥4 months, the ORR and CR rates were comparable to magrolimab.
- Previous Study: Magrolimab achieved 91% ORR and 42% CR in 33 MDS patients.
- Future Plans: I-Mab expects to present detailed results in 2H22 and plans to initiate a registrational trial in MDS this year.
- Potential: Due to comparable efficacy and better safety profile, leMZoparlimab is expected to become an FIC & BIC CD47 antibody.
2. Commercialization Strategy
- Phase 2/3 Assets: I-Mab expects to complete three near-term BLA filings and product launches in 2023-2025 in China.
- Key Candidates: Felzartamab (CD38), eftansomatropin alfa (long-acting growth hormone), and potentially leMZoparlimab (CD47).
- Manufacturing: A new local manufacturing plan for felzartamab is in place, with NDA filing planned for 2022 for treatment of 3L MM.
- Facility Expansion: Phase One facility (6,000L) operational by June 2022, Phase Two (32,000L) construction expected to be completed by 2024.
3. Uliledlimab (CD73)
- Phase 2 Basket Trial: In combination with toripalimab (NCT04322006), ongoing in China for solid tumor patients.
- Key Results: Preliminary data expected to be released at the 2022 ASCO meeting, which could lead to a license-out deal.
Strategic Initiatives
- Listing in HKEx: Accelerated to mitigate US delisting risks.
- Accounting Audit: Plans to hire an accounting firm subject to PCAOB inspection starting in 2022.
- In-License Opportunities: Negotiating to in-license a pre-BLA product in the hematologic malignancy space to expand its portfolio.
Financial Projections (DCF Valuation)
-
FCFF (RMB mn):
- 2022E: (1,797)
- 2023E: (860)
- 2024E: (328)
- 2025E: 401
- 2026E: 1,599
- 2027E: 2,831
- 2028E: 3,426
- 2029E: 4,116
- 2030E: 4,671
- 2031E: 5,469
- 2032E: 5,618
- 2033E: 5,974
- 2034E: 6,035
- Terminal Value (2035E): 122,997 RMB mn
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Equity Value (US$ mn):
- 2022E: 8,280
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WACC: 9.4%
-
Terminal Growth Rate: 4.0%
Key Ratios
-
Gross Margin:
- FY20A: 100%
- FY21A: 100%
- FY22E: 85%
- FY23E: 86%
- FY24E: 87%
-
Current Ratio (x):
- FY20A: 9
- FY21A: 8
- FY22E: 95
- FY23E: 51
- FY24E: 27
-
ROE:
- FY20A: 8%
- FY21A: (51)%
- FY22E: (35)%
- FY23E: (30)%
- FY24E: 8%
-
ROA:
- FY20A: 7%
- FY21A: (41)%
- FY22E: (31)%
- FY23E: (25)%
- FY24E: 6%
Share Performance
- Market Cap (US$ mn): 1,515
- Avg. 3mths t/o (US$ mn): 22.01
- 52W High/Low (US$): 85.40/12.00
- Total Issued Shares (mn): 80
- Share Performance:
- 1-mth: -23.3%
- 3-mth: -60.4%
- 6-mth: -73.9%
Shareholding Structure
- Hillhouse Capital: 8.99%
- GIC: 5.89%
- Tasly Pharma: 5.44%
- Founder: 5.40%
- Genexine: 4.62%
- Rowe Price: 4.17%
- Others: 65.49%
Analyst Ratings
- CMBIGM Rating: BUY
- Target Price: US$103.60
- 12-Month Return Potential: Over 15%
Risk and Disclaimer
- The report is based on publicly available information and may not be suitable for all investors.
- CMBIGM does not provide individually tailored investment advice.
- Past performance does not guarantee future results.
- The report is for informational purposes only and should not be construed as an offer or solicitation to buy or sell securities.
- There are potential conflicts of interest and the report is not liable for any losses incurred from reliance on its contents.
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