Close
CDMO Safety Testing 2026
Novotech

Antihypertensive drug Micatrio combination tablets launch in Japan

Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access the Media Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Related stories

Bioprocess Analytics Improving Biologics Manufacturing

The immense complexity of modern biopharmaceutical production is being navigated through the strategic and systematic application of bioprocess analytics improving biologics manufacturing. By leveraging real-time data streams and advanced monitoring tools, manufacturers can gain a granular, molecular-level understanding of cellular behavior and the surrounding environmental conditions within the bioreactor. This proactive, data-driven approach allows for immediate, automated adjustments that optimize therapeutic yield, ensure absolute product consistency, and significantly streamline the arduous path toward commercial-scale production in a highly regulated global environment.

Cell Therapy Quality Control Improving Clinical Outcomes

The long-term success of advanced medicinal products is fundamentally dependent on a rigorous and comprehensive approach to cell therapy quality control improving clinical outcomes. By implementing stringent, multi-stage testing for identity, purity, potency, and safety, manufacturers can guarantee that every individual dose delivered to a patient meets the highest possible standards of GMP compliance. This systematic and data-driven oversight minimizes clinical risks and enhances the reproducibility of complex treatments, ultimately leading to more predictable and successful therapeutic results in the rapidly evolving field of regenerative medicine.

GMP Cytokines Advancing Cell Therapy Manufacturing

The rapid transition of cell-based treatments from the experimental laboratory stage to the standard of clinical care is being enabled by the availability of GMP cytokines advancing cell therapy manufacturing. These vital signaling molecules are absolutely essential for the successful expansion, specific differentiation, and functional activation of therapeutic cell populations, such as CAR T cells used in oncology. By strictly adhering to Good Manufacturing Practice standards, suppliers ensure that these critical raw materials possess the high purity, consistent potency, and clinical safety required for human applications, thereby reducing product variability and significantly enhancing the success rate of regenerative medicine.
- Advertisement -

Nippon Boehringer Ingelheim Co., Ltd. and Astellas Pharma Inc. announced that the companies have newly launched “Micatrio®Combination Tablets,” a combination drug of “Micardis® Tablets” (AT1 receptor blocker [ARB]), long-acting calcium channel blocker (CCB) amlodipine besylate and the thiazide diuretic hydrochlorothiazide (HCTZ).

Hypertension is a major risk factor for cardiovascular death, yet the rate of the patient undergoing treatment and keeping their blood pressure under control remains at approximately 30% for men and approximately 40% for women.  By increasing the medication adherence, the combination drug is expected to improve the rate to achieve a target blood pressure.1 The newly launched “Micatrio® Combination Tablets” is the first combination drug in Japan to contain the three ingredients of a renin-angiotensin inhibitor, a CCB and small dose diuretic.  Compared to ARB/CCB combination formulations and ARB/HCTZ combination formulations, it is expected to have a strong antihypertensive effect that lasts for 24 hours. 

“Micatrio® Combination Tablets” constitute the Micardis® family along with “Micardis® 20mg/40mg/80mg Tablets”, “Micombi® Combination Tablets AP/BP”, a combination drug with HCTZ and “Micamlo®Combination Tablets AP/BP,” a combination drug with the long-acting CCB amlodipine besylate (telmisartan formulations).In addition, “Micatrio® Combination Tablets,” like the other telmisartan formulations, will be manufactured by Nippon Boehringer Ingelheim, distributed by Astellas and co-promoted by both companies. Nippon Boehringer Ingelheim and Astellas remain committed to further contribute to hypertension treatment through the Micardis family.

Overview of “Micatrio® Combination Tablets” 
Date of Launch: November 18, 2016
Date of Price Listing: November 18, 2016
Date of Approval:September 28, 2016
Brand Name: Micatrio® Combination Tablets
Generic Name: Telmisartan/amlodipine besylate/hydrochlorothiazide
Dosage Form/Content: Film-coated tablet containing 80 mg, 5 mg and 12.5 mg of telmisartan, amlodipine, and hydrochlorothiazide per tablet, respectively

About Telmisartan
Telmisartan is a drug that was discovered and developed by Boehringer Ingelheim.  In Japan, telmisartan is available as Micardis® Tablets 20 mg / 40 mg / 80 mg, Micombi® Combination Tablets AP/BP, a combination drug with HCTZ, and Micamlo® Combination Tablets AP/BP, a combination drug with the long-acting CCB amlodipine besilate. These drugs comprise the Micardis® family of products including Micatrio.  They are number one in terms of sales in the ARB family in Japan2.  In ONTARGET3, the largest ARB clinical study published in 2008, it was reported to have effectiveness for suppressing cardiovascular events equivalent to ACE inhibitor Ramipril (unapproved in Japan).

World Pharma Today brings together the global pharmaceutical industry — from R&D leaders and regulatory affairs professionals to manufacturers and distribution executives — through trusted editorial, market intelligence, and digital engagement.

Our 2026 Media Pack offers integrated solutions to reach your audience:

  • Magazine & Digital Editions Showcase your brand within premium pharmaceutical industry coverage read by executives and decision - makers worldwide.
  • Industry Insights & Reports Align with data - driven analysis, trend reports, and regional roundups across the global pharmaceutical and life sciences value chain.
  • Brand Authority & Credibility Position your company as a thought leader through expert commentary, interviews, and special features.

Latest stories

Related stories

Bioprocess Analytics Improving Biologics Manufacturing

The immense complexity of modern biopharmaceutical production is being navigated through the strategic and systematic application of bioprocess analytics improving biologics manufacturing. By leveraging real-time data streams and advanced monitoring tools, manufacturers can gain a granular, molecular-level understanding of cellular behavior and the surrounding environmental conditions within the bioreactor. This proactive, data-driven approach allows for immediate, automated adjustments that optimize therapeutic yield, ensure absolute product consistency, and significantly streamline the arduous path toward commercial-scale production in a highly regulated global environment.

Cell Therapy Quality Control Improving Clinical Outcomes

The long-term success of advanced medicinal products is fundamentally dependent on a rigorous and comprehensive approach to cell therapy quality control improving clinical outcomes. By implementing stringent, multi-stage testing for identity, purity, potency, and safety, manufacturers can guarantee that every individual dose delivered to a patient meets the highest possible standards of GMP compliance. This systematic and data-driven oversight minimizes clinical risks and enhances the reproducibility of complex treatments, ultimately leading to more predictable and successful therapeutic results in the rapidly evolving field of regenerative medicine.

GMP Cytokines Advancing Cell Therapy Manufacturing

The rapid transition of cell-based treatments from the experimental laboratory stage to the standard of clinical care is being enabled by the availability of GMP cytokines advancing cell therapy manufacturing. These vital signaling molecules are absolutely essential for the successful expansion, specific differentiation, and functional activation of therapeutic cell populations, such as CAR T cells used in oncology. By strictly adhering to Good Manufacturing Practice standards, suppliers ensure that these critical raw materials possess the high purity, consistent potency, and clinical safety required for human applications, thereby reducing product variability and significantly enhancing the success rate of regenerative medicine.

Recombinant Proteins Driving Biologics Innovation

The landscape of modern therapeutic development is being fundamentally reshaped by the precision of recombinant proteins driving biologics innovation. These highly engineered molecules serve as the foundational architecture for initial drug discovery, the creation of sophisticated high-throughput assay development, and the eventual transition into large-scale biologics manufacturing. By utilizing advanced protein expression platforms, the pharmaceutical industry can now produce specific, high-purity proteins that effectively mimic complex natural biological functions with extraordinary accuracy, ensuring that new treatments are both safe and potent for global distribution.

Subscribe

- Never miss a story with notifications

- Gain full access to our premium content

- Browse free from any location or device.

Media Packs

Expand Your Reach With Our Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results!

– Access theMedia Pack Now

– Book a Conference Call

Leave Message for Us to Get Back

Translate »