Significant ETF Inflows: SCHV, DIS, PEP, AMGN
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Sep 05 2025
0mins
Should l Buy AMGN?
Source: NASDAQ.COM
52-Week Range of SCHV: SCHV's share price has a 52-week low of $23.08 and a high of $28.88, with the last trade recorded at $28.67, indicating its current position within this range.
Understanding ETFs: Exchange traded funds (ETFs) function like stocks, where investors buy and sell "units" that can be created or destroyed based on demand, affecting the underlying holdings and market dynamics.
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Analyst Views on AMGN
Wall Street analysts forecast AMGN stock price to fall
19 Analyst Rating
11 Buy
7 Hold
1 Sell
Moderate Buy
Current: 366.200
Low
272.00
Averages
345.87
High
425.00
Current: 366.200
Low
272.00
Averages
345.87
High
425.00
About AMGN
Amgen Inc. is a biotechnology company. It discovers, develops, manufactures and delivers medicines for the toughest diseases. It focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve people’s lives. It operates in the human therapeutics segment. Its marketed products portfolio includes EPOGEN (epoetin alfa); Aranesp (darbepoetin alfa); Parsabiv (etelcalcetide); Neulasta (pegfilgrastim); KANJINTI (trastuzumab-anns); Otezla; BLINCYTO (blinatumomab); ACTIMMUNE (interferon gamma-1b); Neulasta (pegfilgrastim); Sensipar/Mimpara (cinacalcet); Prolia (denosumab); ENBREL; QUINSAIR (levofloxacin); Repatha (evolocumab) and others. It markets ENBREL, a tumor necrosis factor blocker, in the United States and Canada. It markets Otezla, a small molecule that inhibits phosphodiesterase 4, in many countries around the world. It markets Repatha, a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor, in many countries around the world.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
UPLIZNA Approved in Europe for Myasthenia Gravis Treatment
- First Therapy Approved: UPLIZNA (inebilizumab) is the first therapy approved by the European Commission for treating generalized myasthenia gravis (gMG) in adults with positive AChR and MuSK antibodies, offering a new long-term control option that is expected to significantly enhance patient quality of life.
- Clinical Trial Success: In the MINT study, 87.4% of patients receiving UPLIZNA successfully reduced their steroid dosage to 5 mg per day or less, demonstrating its effectiveness in minimizing steroid dependency and potentially reducing long-term side effects associated with steroid use.
- Convenient Treatment Regimen: UPLIZNA's administration schedule of twice a year after two initial doses allows for sustained disease control, which may improve patient adherence and treatment outcomes due to its convenience.
- Broad Market Potential: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also positions the drug to capture significant market share, especially as the prevalence of gMG continues to rise globally.
See More
UPLIZNA Approved for Adult gMG Treatment in Europe
- New Therapy Approval: UPLIZNA (Inebilizumab) has been approved by the European Commission as an adjunct treatment for adults with anti-AChR+ and anti-MuSK+ generalized Myasthenia Gravis (gMG), marking a significant advancement in this field.
- Long-term Disease Control: The therapy demonstrates potential for sustained disease control in gMG patients through a biannual maintenance dose following two initial infusions, which may reduce the need for long-term steroid use.
- Clinical Research Support: The approval is based on data from the MINT study, the largest Phase 3 trial for gMG, involving 238 patients, where 87.4% of UPLIZNA patients successfully reduced their steroid dosage to 5mg or less per day by week 26.
- Market Impact: The approval of UPLIZNA provides a new treatment option for gMG patients, expected to enhance patient quality of life while bolstering Amgen's market position in the rare disease sector.
See More
Amgen to Present at 2026 Oncology Leadership Summit
- Event Schedule: Amgen will participate in Citi's 2026 Virtual Oncology Leadership Summit on February 18, 2026, at 12:15 p.m. PT, where Jean-Charles Soria, Senior Vice President of Oncology, will present the company's latest advancements in oncology.
- Webcast Availability: The presentation will be broadcast live over the internet, accessible to media, investors, and the public, ensuring broad dissemination of information, and will be archived on Amgen's website for at least 90 days for later viewing.
- Company Background: Founded over 45 years ago, Amgen is dedicated to discovering, developing, and manufacturing innovative medicines targeting cancer, heart disease, inflammatory conditions, rare diseases, and obesity, continuously pushing the boundaries of the biotechnology industry and showcasing strong market competitiveness.
- Industry Recognition: Amgen has been recognized for its innovation and workplace culture by Fast Company and Forbes, and is a constituent of the Dow Jones Industrial Average and Nasdaq-100 Index, highlighting its leadership and influence in the biopharmaceutical sector.
See More
Amgen to Present at Citi's 2026 Virtual Oncology Leadership Summit
- Event Schedule: Amgen will participate in Citi's Virtual Oncology Leadership Summit on February 18, 2026, at 12:15 PM PT, featuring a presentation by Jean-Charles Soria, Senior Vice President of Oncology, highlighting the company's advancements in oncology.
- Webcast Availability: The presentation will be broadcast live over the internet, accessible to media, investors, and the general public, ensuring broad audience engagement and enhancing the company's transparency and public involvement.
- Replay Feature: Following the live event, the presentation will be archived and available for replay for at least 90 days, allowing investors and the public who missed the live session to access the information, thereby improving information accessibility and dissemination.
- Company Background: With over 45 years of experience, Amgen focuses on developing innovative medicines to tackle major diseases globally, leveraging its leadership in biotechnology to advance treatments for cancer, heart disease, and more, showcasing strong market competitiveness and innovation capabilities.
See More
UPLIZNA Approved by EU for Myasthenia Gravis Treatment
- New Therapy Approval: Amgen's UPLIZNA (inebilizumab) has received EU approval as a new treatment option for adults with generalized myasthenia gravis (gMG), particularly for patients who are positive for AChR+ and MuSK+ antibodies, marking a significant advancement in the treatment landscape.
- Hope for Patients: With a dosing regimen of twice a year following two initial doses, UPLIZNA offers the potential for long-term disease control, which could significantly improve patients' quality of life and reduce reliance on steroids.
- Clinical Trial Support: The approval is supported by results from the MINT trial, the largest Phase 3 clinical trial for gMG, which demonstrated that 87.4% of UPLIZNA patients reduced their steroid dosage to 5mg or less daily by week 26, showcasing the drug's efficacy.
- Broad Market Potential: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also has the potential to drive market share growth for Amgen in the rare disease sector, further solidifying its leadership position in the biopharmaceutical industry.
See More
UPLIZNA Approved in Europe for gMG Treatment
- New Therapy Approval: Amgen's UPLIZNA (inebilizumab) has been approved by the European Commission as an adjunct treatment for adults with anti-AChR+ and anti-MuSK+ generalized myasthenia gravis (gMG), marking a significant advancement in treatment options.
- Hope for Patients: The drug offers the potential for long-term disease control through a biannual maintenance dose, which may reduce patients' reliance on long-term steroids, thereby improving their quality of life.
- Clinical Trial Support: The approval is backed by results from the MINT study, which showed that 87.4% of patients reduced their steroid dosage to 5mg or less daily by week 24, demonstrating significant efficacy.
- Broad Market Prospects: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also has the potential to drive Amgen's market share growth in the rare disease sector, further solidifying its leadership in the biopharmaceutical industry.
See More
UPLIZNA Approved in Europe for Myasthenia Gravis Treatment
- First Therapy Approved: UPLIZNA (inebilizumab) is the first therapy approved by the European Commission for treating generalized myasthenia gravis (gMG) in adults with positive AChR and MuSK antibodies, offering a new long-term control option that is expected to significantly enhance patient quality of life.
- Clinical Trial Success: In the MINT study, 87.4% of patients receiving UPLIZNA successfully reduced their steroid dosage to 5 mg per day or less, demonstrating its effectiveness in minimizing steroid dependency and potentially reducing long-term side effects associated with steroid use.
- Convenient Treatment Regimen: UPLIZNA's administration schedule of twice a year after two initial doses allows for sustained disease control, which may improve patient adherence and treatment outcomes due to its convenience.
- Broad Market Potential: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also positions the drug to capture significant market share, especially as the prevalence of gMG continues to rise globally.
See More
UPLIZNA Approved for Adult gMG Treatment in Europe
- New Therapy Approval: UPLIZNA (Inebilizumab) has been approved by the European Commission as an adjunct treatment for adults with anti-AChR+ and anti-MuSK+ generalized Myasthenia Gravis (gMG), marking a significant advancement in this field.
- Long-term Disease Control: The therapy demonstrates potential for sustained disease control in gMG patients through a biannual maintenance dose following two initial infusions, which may reduce the need for long-term steroid use.
- Clinical Research Support: The approval is based on data from the MINT study, the largest Phase 3 trial for gMG, involving 238 patients, where 87.4% of UPLIZNA patients successfully reduced their steroid dosage to 5mg or less per day by week 26.
- Market Impact: The approval of UPLIZNA provides a new treatment option for gMG patients, expected to enhance patient quality of life while bolstering Amgen's market position in the rare disease sector.
See More
Amgen to Present at 2026 Oncology Leadership Summit
- Event Schedule: Amgen will participate in Citi's 2026 Virtual Oncology Leadership Summit on February 18, 2026, at 12:15 p.m. PT, where Jean-Charles Soria, Senior Vice President of Oncology, will present the company's latest advancements in oncology.
- Webcast Availability: The presentation will be broadcast live over the internet, accessible to media, investors, and the public, ensuring broad dissemination of information, and will be archived on Amgen's website for at least 90 days for later viewing.
- Company Background: Founded over 45 years ago, Amgen is dedicated to discovering, developing, and manufacturing innovative medicines targeting cancer, heart disease, inflammatory conditions, rare diseases, and obesity, continuously pushing the boundaries of the biotechnology industry and showcasing strong market competitiveness.
- Industry Recognition: Amgen has been recognized for its innovation and workplace culture by Fast Company and Forbes, and is a constituent of the Dow Jones Industrial Average and Nasdaq-100 Index, highlighting its leadership and influence in the biopharmaceutical sector.
See More
Amgen to Present at Citi's 2026 Virtual Oncology Leadership Summit
- Event Schedule: Amgen will participate in Citi's Virtual Oncology Leadership Summit on February 18, 2026, at 12:15 PM PT, featuring a presentation by Jean-Charles Soria, Senior Vice President of Oncology, highlighting the company's advancements in oncology.
- Webcast Availability: The presentation will be broadcast live over the internet, accessible to media, investors, and the general public, ensuring broad audience engagement and enhancing the company's transparency and public involvement.
- Replay Feature: Following the live event, the presentation will be archived and available for replay for at least 90 days, allowing investors and the public who missed the live session to access the information, thereby improving information accessibility and dissemination.
- Company Background: With over 45 years of experience, Amgen focuses on developing innovative medicines to tackle major diseases globally, leveraging its leadership in biotechnology to advance treatments for cancer, heart disease, and more, showcasing strong market competitiveness and innovation capabilities.
See More
UPLIZNA Approved by EU for Myasthenia Gravis Treatment
- New Therapy Approval: Amgen's UPLIZNA (inebilizumab) has received EU approval as a new treatment option for adults with generalized myasthenia gravis (gMG), particularly for patients who are positive for AChR+ and MuSK+ antibodies, marking a significant advancement in the treatment landscape.
- Hope for Patients: With a dosing regimen of twice a year following two initial doses, UPLIZNA offers the potential for long-term disease control, which could significantly improve patients' quality of life and reduce reliance on steroids.
- Clinical Trial Support: The approval is supported by results from the MINT trial, the largest Phase 3 clinical trial for gMG, which demonstrated that 87.4% of UPLIZNA patients reduced their steroid dosage to 5mg or less daily by week 26, showcasing the drug's efficacy.
- Broad Market Potential: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also has the potential to drive market share growth for Amgen in the rare disease sector, further solidifying its leadership position in the biopharmaceutical industry.
See More
UPLIZNA Approved in Europe for gMG Treatment
- New Therapy Approval: Amgen's UPLIZNA (inebilizumab) has been approved by the European Commission as an adjunct treatment for adults with anti-AChR+ and anti-MuSK+ generalized myasthenia gravis (gMG), marking a significant advancement in treatment options.
- Hope for Patients: The drug offers the potential for long-term disease control through a biannual maintenance dose, which may reduce patients' reliance on long-term steroids, thereby improving their quality of life.
- Clinical Trial Support: The approval is backed by results from the MINT study, which showed that 87.4% of patients reduced their steroid dosage to 5mg or less daily by week 24, demonstrating significant efficacy.
- Broad Market Prospects: The approval of UPLIZNA not only provides a new treatment option for gMG patients but also has the potential to drive Amgen's market share growth in the rare disease sector, further solidifying its leadership in the biopharmaceutical industry.
See More
