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'UTM Rocketry Team' Creates History By Reaching IREC 2025 Finals

'UTM Rocketry Team' Creates History By Reaching IREC 2025 Finals

Barnama13-06-2025

JOHOR BAHRU, June 13 (Bernama) -- A group of Universiti Teknologi Malaysia (UTM) students created history by launching their homemade rocket "RIMAU-1" in the International Rocket Engineering Competition (IREC) 2025, currently taking place in Midland, Texas, in the United States.
UTM said in a statement that this achievement makes the university the first Malaysian team to advance to the final stages of this prestigious six-day competition, organised by the Tripoli Rocketry Association, which is ending tomorrow (June 14) thereby bringing honour to the country on the global stage.
According to the statement, the team known as the UTM Rocketry Team, led by mechanical engineering final-year student T K Arykummara together with teammates Brenden Huang Hong Quan, K Raahull, Izzat Idlan Amir Raslan and S N Shivee Prakkaash, who represent a combination of students from the mechanical engineering and electrical engineering faculties.
"Interestingly, the team also developed a rocket parachute system as a safety measure, in addition to using ammonium perchlorate as the main propulsion system to reach the target altitude of 3,000 metres (m) in Texas airspace.
"In addition, the cost of constructing RIMAU-1 is estimated at RM40,000, while the total cost including travel and logistics reaches RM200,000. (Moreover) this project also received support and financial assistance from the Faculty of Mechanical Engineering, the Office of the Deputy Vice-Chancellor for Student Affairs (JTNCHEPA), UTM International (UTMI) as well as several other sources," said the statement.
Meanwhile, Arykummara in the same statement said the rocket named RIMAU-1, which is 2.8 m in height and weighs 28 kilogrammes, was built using fiberglass and carbon material, and is expected to reach a maximum height of up to 3,000 m in accordance with the height requirements set by the organisers.
He said the process to build the rocket was not just about assembling components but involved intensive research, repeated testing, and meticulous attention to every technical and safety aspect.
"The handmade rocket took a total of more than nine months to build and was the result of teamwork, consisting of 40 people from various technical disciplines. The project began early testing in January and was only seriously worked on starting in March, with an intensive two-month construction period.
"Therefore, this participation is not just a competition, but a symbol of our team's spirit of innovation, resilience, and cooperation bringing the Malaysian spirit to the international stage," said Arykummara.

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Full Results Orforglipron 3 mg Orforglipron 12 mg Orforglipron 36 mg Placebo Primary Endpoint A1C reduction from baseline of 8.0 %i Efficacy estimand 1.3 % 1.6 % 1.5 % 0.1 % Treatment-regimen estimand4 1.2 % 1.5 % 1.5 % 0.4 % Key Secondary Endpointsii Percent weight reduction from baseline of 90.2 kg (198.9 lbs)i,iii Efficacy estimand 4.7 % 6.1 % 7.9 % 1.6 % Treatment-regimen estimand 4.5 % 5.8 % 7.6 % 1.7 % Weight reduction from baseline of 90.2 kg (198.9 lbs)i,iii Efficacy estimand 4.4 kg (9.7 lbs) 5.5 kg (12.2 lbs) 7.3 kg (16.0 lbs) 1.3 kg (2.9 lbs) Treatment-regimen estimand 4.2 kg (9.3 lbs) 5.2 kg (11.5 lbs) 7.2 kg (15.8 lbs) 1.5 kg (3.4 lbs) Percent of participants achieving A1C <7 %i Efficacy estimand 72.9 % 76.2 % 74.9 % 28.0 % Treatment-regimen estimand 68.1 % 72.9 % 72.7 % 33.0 % Percent of participants achieving A1C ≤6.5 %i,ii Efficacy estimand 61.5 % 62.3 % 66.0 % 13.5 % Treatment-regimen estimand 56.9 % 58.1 % 61.9 % 14.9 % Percent of participants achieving A1C <5.7 %iii Efficacy estimand 17.7 % 25.8 % 23.9 % 3.8 % Treatment-regimen estimand 16.8 % 23.9 % 21.5 % 3.8 % Fasting serum glucose reduction from baseline of 147.5 mg/dLi Efficacy estimand 30.6 mg/dL 37.4 mg/dL 37.8 mg/dL 1.1 mg/dL Treatment-regimen estimand 30.7 mg/dL 36.5 mg/dL 34.7 mg/dL 10.8 mg/dL iSuperiority test was adjusted for from the full list of key secondary endpoints are available in the of participants achieving A1C <5.7% across all orforglipron doses and body weight for orforglipron 3 mg were not controlled for Type 1 error. 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ATTAIN-1 and ATTAIN-2, evaluating orforglipron for weight management, will also be shared in the third quarter of this year. Lilly remains on track to submit orforglipron for weight management to global regulatory agencies by the end of this year and for the treatment of type 2 diabetes in 2026. About orforglipron Orforglipron (or-for-GLIP-ron) is an investigational, once-daily small molecule (non-peptide) oral glucagon-like peptide-1 receptor agonist that can be taken any time of the day without restrictions on food and water intake.5 Orforglipron was discovered by Chugai Pharmaceutical Co., Ltd. and licensed by Lilly in 2018. Chugai and Lilly published the preclinical pharmacology data of this molecule together.6 Lilly is running Phase 3 studies on orforglipron for the treatment of type 2 diabetes and for weight management in adults with obesity or overweight with at least one weight-related medical problem. It is also being studied as a potential treatment for obstructive sleep apnea and hypertension in adults with obesity. About ACHIEVE-1 and the ACHIEVE clinical trial program ACHIEVE-1 (NCT05971940) is a Phase 3, 40-week, randomized, double-blind, placebo-controlled trial comparing the efficacy and safety of orforglipron 3 mg, 12 mg and 36 mg as monotherapy to placebo in adults with type 2 diabetes and inadequate glycemic control with diet and exercise alone. The trial randomized 559 participants across the U.S., China, India, Japan and Mexico in 1:1:1:1 ratio to receive either 3 mg, 12 mg or 36 mg orforglipron or placebo. The primary objective of the study was to demonstrate that orforglipron (3 mg, 12 mg, 36 mg) is superior in A1C reduction from baseline after 40 weeks, compared to placebo, in people with type 2 diabetes who have not taken any anti-diabetic medications for at least 90 days prior to visit 1, and are naïve to insulin therapy. Study participants had a HbA1c between ≥7.0% and ≤9.5% and a BMI of ≥23 kg/m2. All participants in the orforglipron treatment arms started the study at a dose of orforglipron 1 mg once-daily and then increased the dose in a step-wise approach at four-week intervals to their final randomized maintenance dose of 3 mg (via a 1 mg step), 12 mg (via steps at 1 mg, 3 mg and 6 mg) or 36 mg (via steps at 1 mg, 3 mg, 6 mg, 12 mg and 24 mg). Flexible dosing was not permitted. The ACHIEVE Phase 3 global clinical development program for orforglipron has enrolled more than 6,000 people with type 2 diabetes across five global registration trials. The program began in 2023 with results anticipated later this year and into 2026. About LillyLilly is a medicine company turning science into healing to make life better for people around the world. We've been pioneering life-changing discoveries for nearly 150 years, and today our medicines help tens of millions of people across the globe. Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing new discoveries to solve some of the world's most significant health challenges: redefining diabetes care; treating obesity and curtailing its most devastating long-term effects; advancing the fight against Alzheimer's disease; providing solutions to some of the most debilitating immune system disorders; and transforming the most difficult-to-treat cancers into manageable diseases. With each step toward a healthier world, we're motivated by one thing: making life better for millions more people. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. To learn more, visit and or follow us on Facebook, Instagram and LinkedIn. P-LLY The efficacy estimand represents the treatment effect had on all participants who adhered to the study drug (with possible dose interruptions) for 40 weeks without initiating additional antihyperglycemic medications (>14 days of use). American Diabetes Association. Standards of Care in Diabetes—2020 Abridged for Primary Care Providers. Clinical Diabetes 2020; 38(1):10–38. Percent of participants achieving A1C <5.7% across all doses was not controlled for Type 1 error. The treatment-regimen estimand represents the estimated average treatment effect regardless of treatment discontinuation or initiation of additional antihyperglycemic medications. Ma X, Liu R, Pratt EJ, Benson CT, Bhattachar SN, Sloop KW. Effect of Food Consumption on the Pharmacokinetics, Safety, and Tolerability of Once-Daily Orally Administered Orforglipron (LY3502970), a Non-peptide GLP-1 Receptor Agonist. Diabetes Ther. 2024 Apr;15(4):819-832. Epub 2024 Feb 24. PMID: 38402332; PMCID: PMC10951152. T. Kawai, B. Sun, H. Yoshino, D. Feng, Y. Suzuki, M. Fukazawa, S. Nagao, D.B. Wainscott, A.D. Showalter, B.A. Droz, T.S. Kobilka, M.P. Coghlan, F.S. Willard, Y. Kawabe, B.K. Kobilka, & K.W. Sloop, Structural basis for GLP-1 receptor activation by LY3502970, an orally active nonpeptide agonist, Proc. Natl. Acad. Sci. U.S.A. 117 (47) 29959-29967, (2020). Cautionary Statement Regarding Forward-Looking Statements This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about orforglipron as a potential treatment for adults with type 2 diabetes, and the timeline for future readouts, presentations, and other milestones relating to orforglipron and its clinical trials and reflects Lilly's current beliefs and expectations. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of drug research, development, and commercialization. Among other things, there is no guarantee that planned or ongoing studies will be completed as planned, that future study results will be consistent with study results to date, that orforglipron will prove to be a safe and effective treatment for type 2 diabetes, that orforglipron will receive regulatory approval, or that Lilly will execute its strategy as expected. For further discussion of these and other risks and uncertainties that could cause actual results to differ from Lilly's expectations, see Lilly's Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release. Trademarks and Trade Names All trademarks or trade names referred to in this press release are the property of the company, or, to the extent trademarks or trade names belonging to other companies are referenced in this press release, the property of their respective owners. Solely for convenience, the trademarks and trade names in this press release are referred to without the ® and ™ symbols, but such references should not be construed as any indicator that the company or, to the extent applicable, their respective owners will not assert, to the fullest extent under applicable law, the company's or their rights thereto. We do not intend the use or display of other companies' trademarks and trade names to imply a relationship with, or endorsement or sponsorship of us by, any other companies. Refer to: Brooke Frost; 317-432-9145 (Media) Michael Czapar; czapar_michael_c@ 317-617-0983 (Investors)

Melaka education activist is first M'sian to co-chair international young scientists platform
Melaka education activist is first M'sian to co-chair international young scientists platform

The Star

time12 hours ago

  • The Star

Melaka education activist is first M'sian to co-chair international young scientists platform

MELAKA: A local education activist has become the first Malaysian elected as co-chair of the Global Young Academy (GYA), an international platform representing young scientists across the globe. Associate Professor Dr Sam Chan Siok Yee (pic), a registered pharmacist and academic at Universiti Sains Malaysia's School of Pharmaceutical Sciences, was elected during the GYA's annual general meeting held in Hyderabad, India, from June 10 to 13. The event was officiated by India's Education Minister, Dharmendra Pradhan. Chan will serve alongside returning co-chair, Dr Yensi Flores Bueso of University College Cork, Ireland. Her election followed a hybrid voting process involving over 70 academics from around the world. With her appointment, Malaysia assumes a greater role in shaping the organisation's strategic direction and championing scientific leadership from lower-middle-income countries. In an interview on Saturday (June 21), Chan described the appointment as a 'landmark achievement for Malaysian science and global leadership'. "My elected role marks a significant step forward for gender representation and regional inclusion in global scientific governance,' she said. Chan, 41, said that the position is not merely a personal milestone, but also a recognition of the growing impact of Southeast Asian scientists in the international research community. 'I am deeply honoured to serve as co-chair of the GYA and this role reflects the collective progress of our region's scientific contributions on the world stage,' she said. Founded in 2010, the GYA promotes international, interdisciplinary, and intergenerational dialogue to address pressing global challenges. The academy currently includes 22 Malaysian members who actively contribute to scientific progress. Chan has been involved with the GYA since 2021 and remains committed to strengthening support systems for young researchers worldwide. She also serves as vice-president and education specialist with the Melaka Action Group of Parents in Education (Magpie). According to The Hindu Newspaper (India) on June 16, the GYA's 2025 AGM was held under the theme 'Confluence of Visionaries: Empowering Science for Global Change.' The week-long programme featured sessions on Industry 5.0, human-machine interaction, nutrition and well-being, science-society interfaces and foresight planning. Delegates also contributed to shaping the organisation's future strategic priorities.

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