Markets
News
Analysis
User
24/7
Economic Calendar
Education
Data
- Names
- Latest
- Prev
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
A:--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
A:--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
A:--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
--
F: --
P: --
No matching data
Latest Views
Latest Views
Trending Topics
To quickly learn market dynamics and follow market focuses in 15 min.
In the world of mankind, there will not be a statement without any position, nor a remark without any purpose.
Inflation, exchange rates, and the economy shape the policy decisions of central banks; the attitudes and words of central bank officials also influence the actions of market traders.
Money makes the world go round and currency is a permanent commodity. The forex market is full of surprises and expectations.
Top Columnists
Enjoy exciting activities, right here at FastBull.
The latest breaking news and the global financial events.
I have 5 years of experience in financial analysis, especially in aspects of macro developments and medium and long-term trend judgment. My focus is maily on the developments of the Middle East, emerging markets, coal, wheat and other agricultural products.
BeingTrader chief Trading Coach & Speaker, 8+ years of experience in the forex market trading mainly XAUUSD, EUR/USD, GBP/USD, USD/JPY, and Crude Oil. A confident trader and analyst who aims to explore various opportunities and guide investors in the market. As an analyst I am looking to enhance the trader’s experience by supporting them with sufficient data and signals.
Latest Update
Risk Warning on Trading HK Stocks
Despite Hong Kong's robust legal and regulatory framework, its stock market still faces unique risks and challenges, such as currency fluctuations due to the Hong Kong dollar's peg to the US dollar and the impact of mainland China's policy changes and economic conditions on Hong Kong stocks.
HK Stock Trading Fees and Taxation
Trading costs in the Hong Kong stock market include transaction fees, stamp duty, settlement charges, and currency conversion fees for foreign investors. Additionally, taxes may apply based on local regulations.
HK Non-Essential Consumer Goods Industry
The Hong Kong stock market encompasses non-essential consumption sectors like automotive, education, tourism, catering, and apparel. Of the 643 listed companies, 35% are mainland Chinese, making up 65% of the total market capitalization. Thus, it's heavily influenced by the Chinese economy.
HK Real Estate Industry
In recent years, the real estate and construction sector's share in the Hong Kong stock index has notably decreased. Nevertheless, as of 2022, it retains around 10% market share, covering real estate development, construction engineering, investment, and property management.
Hongkong, China
Ho Chi Minh, Vietnam
Dubai, UAE
Lagos, Nigeria
Cairo, Egypt
White Label
Data API
Web Plug-ins
Affiliate Program
View All
No data
Not Logged In
Log in to access more features
FastBull Membership
Not yet
Purchase
Log In
Sign Up
Hongkong, China
Ho Chi Minh, Vietnam
Dubai, UAE
Lagos, Nigeria
Cairo, Egypt
White Label
Data API
Web Plug-ins
Affiliate Program
Bayer AG BAYRY reported third-quarter 2024 core earnings of 7 cents per American Depositary Receipt (ADR), which missed the Zacks Consensus Estimate of 17 cents. The company reported earnings of 10 cents per ADR in the year-ago quarter.
Core earnings of €0.24 per share deteriorated 36.8% year over year due to impairment losses at the Crop Science division.
Total sales in the reported quarter were $10.9 billion (€9.9 billion), down 3.6% on a reported basis.
On a currency and portfolio-adjusted basis, sales increased 0.6% year over year.
Year to date, shares of Bayer have lost 30.1% against the industry’s growth of 11.6%.
Find the latest EPS estimates and surprises on Zacks Earnings Calendar.
All growth rates mentioned below are on a year-over-year basis after adjusting for currency and portfolio changes.
BAYRY’s Q3 Results in Detail
Bayer reports under three segments, namely Crop Science, Pharmaceuticals and Consumer Health.
In the reported quarter, Crop Science sales decreased 3.6% to €4 billion. Within this segment, Herbicides business was down 11.5% due to volume declines for glyphosate-based products. This was mainly due to purchasing patterns normalizing in Latin and North America.
Fungicides sales were up 13.1% due to increased volumes in all regions. Corn Seed & Traits sales decreased 19.3% due to an overall acreage decline, primarily driven by Latin America. Sales from the Soybean Seed & Traits business declined 2.5% due to a weather-related delay to the start of the season in Latin America. The Insecticides business also grew 9.5%, driven by higher volumes in Latin America. The Vegetable Seeds business recorded encouraging gains that were largely driven by higher volumes and prices in Latin America.
BAYRY’s revenues in the Pharmaceuticals segment increased 2.3% to €4.5 billion. Nubeqa (for cancer) sales surged 83.2% to €417 million, recording gains in all regions and witnessing significant improvements in volumes, especially in the United States and EU. Kerendia sales surged 96.4%, mainly due to a substantial rise in volumes in the United States and business expansion in China.
However, sales of oral anticoagulant Xarelto, co-developed with J&J JNJ, decreased 23% to €802 million due to competitive pressure from generics, especially in Canada and Europe.
In the U.S. market, Xarelto is marketed by J&J. Bayer earns license revenues from JNJ for Xarelto sales in the United States.
Sales of the ophthalmology drug, Eylea, increased 8.6% to €848 million, driven by higher volumes in Europe and Japan as well as a one-time effect of reimbursement in the United Kingdom.
Please note that Bayer’s HealthCare unit co-develops Eylea with Regeneron REGN, which records net product sales of Eylea in the United States. BAYRY records net product sales of Eylea outside the country. REGN records its share of profits/losses in connection with the sales of Eylea outside the United States.
Consumer Health sales rose 5.7% to €1.4 billion, driven by increases in Dermatology (+7.4%) and Pain & Cardio (+10.9%) categories. Dermatology sales gained from continued strong demand for Bepanthen.
Nutritionals (+3.6%) and Allergy & Cold business (+3.1%) also boosted the Consumer Health business.
BAYRY Updates 2024 Guidance
Bayer reiterated its previously provided currency-adjusted guidance for 2024 for the total group. The company expects to generate sales in the range of €47-€49 billion.
However, in view of the weaker-than-anticipated development of the agricultural market, BAYRY revised its forecast for divisional sales. Business performance is below initial expectations at Crop Science and Consumer Health. Nonetheless, Pharmaceuticals division sales is likely to come in at the upper end of the revised guidance.
For the Crop Science Division, Bayer now expects currency and portfolio-adjusted sales growth to decline around 1% to 3% (previous forecast -1% to +3%). For the Pharmaceuticals Division, Bayer expects currency and portfolio-adjusted sales growth to be flat to grow 3% (previous forecast: down -4% to flat year over year). Consumer Health sales growth is projected to increase between 1% and 3% (previous forecast: 3-6%).
Bayer Aktiengesellschaft Price, Consensus and EPS Surprise
Bayer Aktiengesellschaft price-consensus-eps-surprise-chart | Bayer Aktiengesellschaft Quote
Pipeline Updates
In September, BAYRY obtained received regulatory approval for the Eylea 8 mg pre-filled syringe in the European Union.
The company also filed a new drug application (NDA) with the FDA for a third indication for cancer drug Nubeqa (darolutamide) for its use in combination with androgen deprivation therapy (ADT) in patients with metastatic hormone-sensitive prostate cancer (mHSPC).
In October, BAYRY announced that the FDA had accepted the NDA for elinzanetant, an investigational compound for the non-hormonal treatment of moderate to severe vasomotor symptoms associated with menopause.
Our Take on BAYRY's Q3 Perfomance
Although Bayer’s earnings declined in the third quarter due to impairment losses at the Crop Science division, sales growth was encouraging at the Pharmaceutical division. New products, Nubeqa and Kerendia, retained their impressive momentum and offset the negative impact of a decline in Xarelto sales. Consumer Health business, too, posted growth. However, the Crop Science business was adversely impacted by significant declines in glyphosate-based herbicides.
The company is working to expand the labels of its key drugs, Nubeqa and Kerendia, which should boost growth.
Successful drug development is imperative for Bayer amid multiple challenges. The failure of a late-stage study on asundexian was a major setback for the company. BAYRY had earlier slashed dividends to conserve cash as increasing Roundup litigation charges adversely impacted the bottom line.
Bayer's Zacks Rank
BAYRY currently carries a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
Zacks Investment Research
Intellia Therapeutics, Inc. NTLA incurred third-quarter 2024 loss of $1.34 per share, which was narrower than the Zacks Consensus Estimate of a loss of $1.37. In the year-ago quarter, Intellia had incurred a loss of $1.38 per share.
The company’s total revenues currently comprise only collaboration revenues. Intellia reported revenues of $9.1 million for the third quarter of 2024 compared with $12 million reported in the year-ago quarter. Revenues however beat the Zacks Consensus Estimate of $8 million.
The year-over-year decrease in revenues was due to a reduction in revenues related to the AvenCell license and collaboration agreement.
Shares of Intellia have plunged 47.6% year to date compared with the industry’s decline of 2.4%.
Stay up-to-date with all quarterly releases: See Zacks Earnings Calendar.
More on NTLA's Q3 Results
Intellia’s collaboration revenues beat our model estimate of $8 million.
Research and development expenses totaled $123.4 million, up 8.5% from the year-ago quarter’s figure. The increase was due to the advancement of lead pipeline programs.
General and administrative expenses increased around 3.7% year over year to $30.5 million due to an increase in stock-based compensation.
As of Sept 30, 2024, NTLA had cash, cash equivalents and marketable securities worth $944.7 million compared with $939.9 million as of Jun 30, 2024.
NTLA's Recent Pipeline Updates
Intellia has collaborated with Regeneron Pharmaceuticals REGN for the development of its investigational in vivo genome-editing candidate, Nexiguran ziclumeran (nex-z, also known as NTLA-2001).
Nex-z is part of the company’s co-development and co-promotion agreement with Regeneron. While NTLA is the lead party in the deal for nex-z, REGN shares 25% of the development costs and commercial profits.
The phase III MAGNITUDE study is evaluating the safety and efficacy of nex-z in patients with ATTR amyloidosis with cardiomyopathy. Enrollment is currently ongoing in the study.
If the MAGNITUDE study's data are found to be positive, it will enable regulatory filings for the candidate worldwide.
Along with the earnings release, Intellia announced that the FDA has cleared its investigational new drug (IND) application seeking to initiate the pivotal phase III MAGNITUDE-2 study evaluating nex-z for treating hereditary ATTR amyloidosis with polyneuropathy.
The company plans to begin patient enrollment in the MAGNITUDE-2 study outside the United States by 2024-end.
Intellia is developing another pipeline candidate, NTLA-2002, for the treatment of hereditary angioedema (HAE). Last month, the company initiated the pivotal phase III HAELO study evaluating NTLA-2002 for HAE.
The global double-blind, placebo-controlled study will evaluate the safety and efficacy of NTLA-2002 in adults with Type I or Type II HAE. The primary endpoint of the study is to see the change in number of HAE attacks from week five through week 28 of treatment.
Intellia is developing its in vivo gene insertion candidate, NTLA-3001, for the treatment of alpha-1 antitrypsin deficiency (AATD) associated lung disease. The company plans to dose the first patient in a phase I/II study on NTLA-3001 for treating AATD by the end of 2024.
Intellia Therapeutics, Inc. Price, Consensus and EPS Surprise
Intellia Therapeutics, Inc. price-consensus-eps-surprise-chart | Intellia Therapeutics, Inc. Quote
NTLA's Zacks Rank & Other Key Picks
Intellia currently carries a Zacks Rank #2 (Buy).
Some other top-ranked stocks from the biotech sector are Amicus Therapeutics, Inc. FOLD and Castle Biosciences, Inc. CSTL, each carrying a Zacks Rank #1 (Strong Buy) at present. You can see the complete list of today’s Zacks #1 Rank stocks here.
In the past 60 days, estimates for Amicus’ 2024 earnings per share have moved up from 20 cents to 22 cents. Earnings per share estimates for 2025 have improved from 49 cents to 53 cents during the same time. Year to date, shares of FOLD have declined 22.6%.
FOLD’s earnings beat estimates in three of the trailing four quarters while missing on the remaining occasion, the average surprise being 27.09%.
In the past 60 days, estimates for Castle Biosciences’ 2024 loss per share have narrowed from 58 cents to 8 cents. Loss per share estimates for 2025 have narrowed from $2.13 to $1.88 during the same time. Year to date, shares of CSTL have surged 54.4%.
CSTL’s earnings beat estimates in each of the trailing four quarters, the average surprise being 172.72%.
Zacks Investment Research
As the medical breakthroughs progress, biotech stocks are expected to play a significant role in revolutionizing healthcare. Medical advancements in neuroscience and gene therapy have opened up new horizons within this sector.
Therefore, investors looking to benefit from such contribution to the economy might consider biotech stocks, namely, Regeneron Pharmaceuticals, Inc. , Biogen Inc. , and Gilead Sciences, Inc. .
Innovations targeting neurological disorders, such as Alzheimer’s and Parkinson’s, promise to transform treatment approaches by developing therapies that address the underlying causes of these conditions. Several collaborations involving large pharma companies signal a renewed interest in the neuroscience sector. Moreover, the companies are already moving on to early successes in neurotherapeutics, bringing hope to millions of patients.
The expanding field of gene-editing technology is also attracting significant investment interest as companies develop cancer therapies and other targeted treatments. There have been cell and gene therapy advancements like a recombinant AAV vector for glioblastoma treatment, peptide-modified AAV capsids for muscle targeting, and oral delivery systems for oligonucleotides.
So far this year, the FDA has approved 38 cellular and gene therapy products and also 38 novel drugs that target conditions from lung cancer to Alzheimer’s disease and various other chronic ailments. Furthermore, the global biotechnology market is anticipated to reach $4.61 trillion by 2034, growing at a CAGR of 11.5%.
The biotech industry offers an avenue that aligns financial and societal goals, paving the way for transformative impacts in medicine.
With that in mind, let’s delve into the fundamentals of the three Biotech stock picks, starting with the third choice.
Stock #3: Regeneron Pharmaceuticals, Inc. (REGN)
REGN discovers, invents, develops, manufactures, and commercializes medicines for treating various diseases worldwide. The company’s products include EYLEA injection, Dupixent Injection, Libtayo Injection, Praluent Injection, Kevzara Injection, and others.
On November 6, REGN received approval from the European Commission for Dupixent® (dupilumab) to treat eosinophilic esophagitis (EoE) in children aged 1 to 11 years. This approval expands EoE in adults and adolescents, creating a milestone in treating pediatric patients.
On October 18, REGN announced positive data for EYLEA HD® (aflibercept) injection 8 mg from an extension study of the Phase 3 PHOTON trial in patients with diabetic macular edema (DME). It demonstrates continued durable vision and anatomic improvements among 88% of EYLEA HD patients in this phase.
REGN, for the third quarter (ended September 30, 2024), reported total revenues of $3.72 billion, indicating a 10.6% growth from the prior year quarter. Its income from operations increased 6.2% year-over-year to $1.18 billion. The company’s non-GAAP net income came in at $1.46 billion and $12.46 per share, up 10% and 7.5% year-over-year, respectively.
The consensus revenue estimate of $3.63 billion for the fiscal first quarter (ending March 2025) represents a 15.4% increase year-over-year. The consensus EPS estimate of $10.99 for the same quarter indicates a 15.1% improvement year-over-year. The company has an excellent surprise history; it surpassed the consensus revenue and EPS estimates in three of the trailing four quarters.
The stock has surged marginally over the past year to close the last trading session at $829.43.
REGN’s POWR Ratings reflect this robust outlook. The stock has an overall rating of B, which equates to Buy in our proprietary rating system. The POWR Ratings are calculated by considering 118 different factors, with each factor weighted to an optimal degree.
REGN has a B grade for Value and Quality. It is ranked #25 out of 328 stocks in the Biotech industry. Click here to see the additional ratings for REGN (Growth, Momentum, Stability, and Sentiment).
Stock #2: Biogen Inc. (BIIB)
BIIB is a global biopharmaceutical company focused on discovering, developing, and delivering advanced therapies for people living with serious and complex diseases worldwide. The company has a portfolio of medicines to treat multiple sclerosis (MS), spinal muscular atrophy (SMA), Alzheimer's disease, and amyotrophic lateral sclerosis (ALS).
On October 29, BIIB and Neomorph Inc. collaborated on research to discover and develop molecular glue degraders for Alzheimer’s, rare neurological and immunological diseases. This collaboration is under the terms where Neomorph's molecular glue degrader platform and BIIB’s expertise with cutting-edge innovation will be able to create a meaningful therapy for the patients.
In the same month, BIIB received Breakthrough Therapy Designation (BTD) from the U.S. Food and Drug Administration (FDA) for felzartamab, an investigational anti-CD38 monoclonal antibody. It is used to treat late antibody-mediated rejection (AMR) without T-cell mediated rejection in kidney transplant patients. This designation will enhance the efficiency in the development of the antibody.
For the third quarter of 2024, which ended on September 30, BIIB’s total revenues stood at $1.77 billion. The company’s net income stood at $388.50 million compared to the prior-year quarter’s loss of $68.10 million, while its EPS came in at $2.66 versus a loss of $0.47 per share last year. In addition, BIIB’s adjusted free cash flow rose 73.8% from the year-ago value to $900.60 million.
Per the updated financial guidance for the full year 2024, BIIB now forecasts non-GAAP EPS between $16.10 and $16.60, up from the previous estimate of $15.75 and $16.25.
Street expects BIIB’s revenue for the fiscal fourth quarter (ending December 2024) to increase 1.2% year-over-year to $2.41 billion. Its EPS for the same period is expected to register a 16.8% growth from the prior year, settling at $3.44. In addition, it surpassed the EPS estimates in three of the trailing four quarters, which is promising.
BIIB’s stock has surged 1.9% intraday to close the last trading session at $176.93.
BIIB’s bright prospects are reflected in its POWR Ratings. The stock has an overall rating of A, which translates to a Strong Buy in our proprietary rating system.
It also has an A grade for Value and a B for Growth and Sentiment. Within the same industry, it is ranked #7 out of 328 stocks. Click here to see BIIB’s ratings for Momentum, Stability, and Quality.
Stock #1: Gilead Sciences, Inc. (GILD)
GILD is a biopharmaceutical company dedicated to advancing treatments for life-threatening diseases such as human immunodeficiency virus (HIV), viral hepatitis, COVID-19, and cancer. Its portfolio of marketed products includes Biktarvy, Genvoya, Odefsey, Truvada, Harvoni, Vemlidy, and Veklury, among others.
On October 2, GILD signed non-exclusive, royalty-free voluntary licensing agreements with six pharmaceutical manufacturers to produce and sell generic lenacapavir (pending regulatory approval) in 120 countries (mainly low- and lower-middle-income) with high HIV incidence. This agreement is to make HIV prevention medicine available worldwide once it is approved.
On September 10, GILD and Genesis Therapeutics, Inc. announced a strategic collaboration to discover and develop novel, small molecule therapies across multiple targets.
This collaboration will utilize Genesis’ advanced AI platform, GEMS, to design and optimize molecules for targets chosen by GILD. The two companies will collaborate on early-stage research, with GILD holding exclusive rights to further develop and market any compounds that come from their joint efforts.
In the fiscal second quarter, which ended on June 30, 2024, GILD’s total revenues increased 5.4% year-over-year to $6.95 billion. The company reported operating income of $2.64 billion, indicating 58.8% growth from the prior-year quarter. GILD’s non-GAAP net income attributable came in at $2.52 billion, up 49.2% year-over-year, while its non-GAAP EPS grew 50% from the year-ago value to $2.01.
According to the full-year guidance, GILD forecasts product sales to range from $27.10 billion to $27.50 billion. The company also expects non-GAAP EPS to be between $3.60 and $3.90, an increase from the previous guidance of $6.85 to $7.25.
Analysts expect GILD’s revenue and EPS for the current year (ending December 2024) to be $27.73 billion and $3.79, respectively. For the fiscal year 2025, both its revenue and EPS are expected to grow by marginally and 91.5% from the prior year to $28.05 billion and $7.26, respectively.
Over the past six months, the stock has gained 39.3%, closing the last trading session at $90.22.
GILD’s strong fundamentals are reflected in its POWR Ratings. It has an overall rating of A, which equates to a Strong Buy in our proprietary rating system.
It has an A grade for Value and a B for Sentiment and Quality. The stock is ranked #4 in the Biotech industry. Click here to access the additional GILD ratings (Growth, Momentum, and Stability).
What To Do Next?
Get your hands on this special report with 3 low priced companies with tremendous upside potential even in today’s volatile markets:
3 Stocks to DOUBLE This Year >
GILD shares were trading at $91.26 per share on Wednesday afternoon, up $1.04 (+1.15%). Year-to-date, GILD has gained 16.28%, versus a 25.37% rise in the benchmark S&P 500 index during the same period.
White Label
Data API
Web Plug-ins
Poster Maker
Affiliate Program
The risk of loss in trading financial instruments such as stocks, FX, commodities, futures, bonds, ETFs and crypto can be substantial. You may sustain a total loss of the funds that you deposit with your broker. Therefore, you should carefully consider whether such trading is suitable for you in light of your circumstances and financial resources.
No decision to invest should be made without thoroughly conducting due diligence by yourself or consulting with your financial advisors. Our web content might not suit you since we don't know your financial conditions and investment needs. Our financial information might have latency or contain inaccuracy, so you should be fully responsible for any of your trading and investment decisions. The company will not be responsible for your capital loss.
Without getting permission from the website, you are not allowed to copy the website's graphics, texts, or trademarks. Intellectual property rights in the content or data incorporated into this website belong to its providers and exchange merchants.